Promoter Variants For Expressing Genes In A Fungal Cell

ABSTRACT

The present invention relates to methods for producing a biological substance, comprising: (a) cultivating a fungal host cell in a medium conducive for the production of the biological substance, wherein the fungal host cell comprises a first nucleic acid sequence encoding the biological substance operably linked to a second nucleic acid sequence comprising a promoter variant selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12; and a subsequence thereof; and hybrid and tandem promoters thereof; and (b) isolating the biological substance from the cultivation medium. The present invention also relates to the isolated promoter variants and to constructs, vectors, and fungal host cells comprising the promoter variants operably linked to nucleic acid sequences encoding biological substances.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No.13/424,018, filed Mar. 19, 2012, which is a divisional of U.S.application Ser. No. 12/054,125, filed Mar. 24, 2008, now U.S. Pat. No.8,138,325, which is a divisional of U.S. application Ser. No.10/716,793, filed Nov. 18, 2003, now U.S. Pat. No. 7,368,262, whichclaims priority from U.S. provisional application Ser. No. 60/427,314,filed Nov. 18, 2002, which applications are fully incorporated herein byreference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to methods for producing biologicalsubstances. The present invention also relates to isolated promotervariants and to nucleic acid constructs, vectors, and host cellscomprising the promoter variants operably linked to nucleic acidsequences encoding biological substances.

2. Description of the Related Art

The recombinant production of a native or heterologous biologicalsubstance in a fungal host cell, particularly a filamentous fungal cellsuch as Aspergillus, may provide for a more desirable vehicle forproducing the substance in commercially relevant quantities.

Recombinant production of a native or heterologous biological substanceis accomplished by constructing an expression cassette in which the DNAcoding for the protein is placed under the expression control of apromoter, excised from a regulated gene, suitable for the host cell. Theexpression cassette is introduced into the host cell, usually byplasmid-mediated transformation. Production of the substance is thenachieved by culturing the transformed host cell under inducingconditions necessary for the proper functioning of the promotercontained on the expression cassette.

The development of a new fungal host cell for the recombinant productionof biological substances generally requires the availability ofpromoters that are suitable for controlling the expression of thesubstances in the host cell. Fusarium venenatum has been shown to beuseful as a new host cell for such expression (WO 96/00787, WO97/26330). Moreover, the promoter from the Fusarium oxysporumtrypsin-like protease gene has been described which is useful forexpressing heterologous genes in Fusarium venenatum host cells (U.S.Pat. No. 5,837,847). U.S. Pat. No. 6,361,973 discloses a glucoamylasepromoter from Fusarium venenatum. However, there is a need in the artfor new promoters for controlling the expression of native andheterologous genes.

It is an object of the present invention to provide improved methods forproducing a biological substance in a fungal host cell and new promotervariants for such production.

SUMMARY OF THE INVENTION

The present invention relates to methods for producing a biologicalsubstance, comprising: (a) cultivating a fungal host cell in a mediumconducive for the production of the biological substance, wherein thefungal host cell comprises a first nucleic acid sequence encoding thebiological substance operably linked to a second nucleic acid sequencecomprising a promoter variant having a nucleic acid sequence selectedfrom the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4,SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9,SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12; and subsequencesthereof; and hybrid and tandem promoters thereof; and (b) isolating thebiological substance from the cultivation medium. The biologicalsubstance may be native or heterologous to the fungal host cell.

The present invention also relates to isolated promoter variantscomprising a nucleic acid sequence selected from the group consisting ofSEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6,SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11,and SEQ ID NO: 12; and subsequences thereof; and hybrid and tandempromoters thereof; and to constructs, vectors, and fungal host cellscomprising one or more of the promoter variants operably linked to anucleic acid sequence encoding a biological substance.

BRIEF DESCRIPTION OF THE FIGURES

FIGS. 1A and B show the DNA sequence of the Fusarium venenatum nativeglucoamylase gene promoter sequence (SEQ ID NO: 1).

FIG. 2 shows a restriction map of pDM237.

FIG. 3 shows a restriction map of pJRoy72.

FIG. 4 shows a restriction map of pNham1.

FIG. 5 shows a restriction map of pNham2.

FIG. 6 shows a restriction map of pDM156.2.

FIG. 7 shows a restriction map of pDM222A.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to methods for producing a biologicalsubstance, comprising (a) cultivating a fungal host cell in a mediumconducive for the production of the biological substance, wherein thefungal host cell comprises a first nucleic acid sequence encoding thebiological substance operably linked to a second nucleic acid sequencecomprising a promoter variant selected from the group consisting of SEQID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ IDNO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, and SEQID NO: 12; and subsequences thereof; and hybrid and tandem promotersthereof; and (b) isolating the biological substance from the cultivationmedium.

In the production methods of the present invention, the cells arecultivated in a nutrient medium suitable for production of thebiological substance using methods known in the art. For example, thecell may be cultivated by shake flask cultivation, small-scale orlarge-scale fermentation (including continuous, batch, fed-batch, orsolid state fermentations) in laboratory or industrial fermentorsperformed in a suitable medium and under conditions allowing thebiological substance to be expressed and/or isolated. The cultivationtakes place in a suitable nutrient medium comprising carbon and nitrogensources and inorganic salts, using procedures known in the art. Suitablemedia are available from commercial suppliers or may be preparedaccording to published compositions (e.g., in catalogues of the AmericanType Culture Collection). If the biological substance is secreted intothe nutrient medium, the substance can be recovered directly from themedium. If the biological substance is not secreted, it can be recoveredfrom cell lysates.

The biological substances may be detected using methods known in the artthat are specific for the biological substances. These detection methodsmay include use of specific antibodies, high performance liquidchromatography, capillary chromatography, formation of an enzymeproduct, disappearance of an enzyme substrate, or SDS-PAGE. For example,an enzyme assay may be used to determine the activity of the enzyme.Procedures for determining enzyme activity are known in the art for manyenzymes (see, for example, D. Schomburg and M. Salzmann (eds.), EnzymeHandbook, Springer-Verlag, New York, 1990).

The resulting biological substance may be isolated by methods known inthe art. For example, a polypeptide of interest may be isolated from thecultivation medium by conventional procedures including, but not limitedto, centrifugation, filtration, extraction, spray-drying, evaporation,or precipitation. The isolated polypeptide may then be further purifiedby a variety of procedures known in the art including, but not limitedto, chromatography (e.g., ion exchange, affinity, hydrophobic,chromatofocusing, and size exclusion), electrophoretic procedures (e.g.,preparative isoelectric focusing (IEF), differential solubility (e.g.,ammonium sulfate precipitation), or extraction (see, e.g., ProteinPurification, J.-C. Janson and Lars Ryden, editors, VCH Publishers, NewYork, 1989). A metabolite of interest may be isolated from a cultivationmedium by, for example, extraction, precipitation, or differentialsolubility, or any method known in the art. The isolated metabolite maythen be further purified using methods suitable for metabolites.

Promoters

The term “promoter” is defined herein as a DNA sequence that binds RNApolymerase and directs the polymerase to the correct downstreamtranscriptional start site of a nucleic acid sequence encoding abiological substance to initiate transcription. RNA polymeraseeffectively catalyzes the assembly of messenger RNA complementary to theappropriate DNA strand of the coding region. The term “promoter” willalso be understood to include the 5′ non-coding region (between promoterand translation start) for translation after transcription into mRNA,cis-acting transcription control elements such as enhancers, and othernucleotide sequences capable of interacting with transcription factors.

The term “promoter variant” is defined herein as a promoter having anucleotide sequence comprising a substitution, deletion, and/orinsertion of one or more nucleotides of a parent promoter, wherein themutant promoter has more or less promoter activity than thecorresponding parent promoter. The term “promoter variant” will alsoencompass natural variants and in vitro generated variants obtainedusing methods well known in the art such as classical mutagenesis,site-directed mutagenesis, and DNA shuffling.

The term “hybrid promoter” is defined herein as parts of two morepromoters that are fused together to generate a sequence that is afusion of the two or more promoters, which when operably linked to acoding sequence mediates the transcription of the coding sequence intomRNA.

The term “tandem promoter” is defined herein as two or more promotersequences each of which is operably linked to a coding sequence andmediates the transcription of the coding sequence into mRNA.

The term “operably linked” is defined herein as a configuration in whicha control sequence, e.g., a promoter sequence, is appropriately placedat a position relative to a coding sequence such that the controlsequence directs the production of a biological substance encoded by thecoding sequence.

The term “coding sequence” is defined herein as a nucleic acid sequencethat is transcribed into mRNA which is translated into a biologicalsubstance, e.g., polypeptide, when placed under the control of theappropriate control sequences. The boundaries of the coding sequence aregenerally determined by the ATG start codon located just upstream of theopen reading frame at the 5′ end of the mRNA and a transcriptionterminator sequence located just downstream of the open reading frame atthe 3′ end of the mRNA. A coding sequence can include, but is notlimited to, genomic DNA, cDNA, semisynthetic, synthetic, and recombinantnucleic acid sequences.

A promoter variant of the present invention may have one or moremutations. Each mutation is an independent substitution, deletion,and/or insertion of a nucleotide. The introduction of a substitution,deletion, and/or insertion of a nucleotide into the promoter may beaccomplished using any of the methods known in the art such as classicalmutagenesis, site-directed mutagenesis, or DNA shuffling. Particularlyuseful is a procedure which utilizes a supercoiled, double stranded DNAvector with an insert of interest and two synthetic primers containingthe desired mutation. The oligonucleotide primers, each complementary toopposite strands of the vector, extend during temperature cycling bymeans of Pfu DNA polymerase. On incorporation of the primers, a mutatedplasmid containing staggered nicks is generated. Following temperaturecycling, the product is treated with Dpnl which is specific formethylated and hemimethylated DNA to digest the parental DNA templateand to select for mutation-containing synthesized DNA. Other proceduresknown in the art may also be used.

The parent promoter of the promoter variants of the present invention isSEQ ID NO: 1 shown in FIGS. 1A and 1B, or the nucleic acid sequencecontained in plasmid pECO3 which is contained in Escherichia coli NRRLB-30067.

The regions chosen for deletion, insertion or substitution of SEQ ID NO:1 were based on observations made about the nucleotide sequence of theFusarium venenatum glucoamylase promoter. At positions, 3792 to 3807,3678 to 3693, and 3814 to 3824 of SEQ ID NO: 1 (U.S. Pat. No.6,361,973), there are regions that share homology to motifs found inother starch inducible fungal promoters. The regions were similar insequence to the IIIa and IIIb regions described previously inAspergillus amylase promoters (Minetoki et al., 1996, Current Genetics30: 432-438). Region IIIa was found in the Aspergillus oryzaealpha-glucosidase, amylase B and glucoamylase promoters as well as inAspergillus niger alpha-glucosidase promoter. Region IIIb was found onlyin the Aspergillus niger and Aspergillus oryzae alpha-glucosidasepromoters. The 3792 to 3807 and 3678 to 3693 regions of the Fusariumvenenatum glucoamlyase promoter have some sequence similarity to theRegion IIIa consensus while the 3814 to 3824 has homology to the IIIbsequence. The analysis of the Aspergillus promoters by Minetoki et al.suggested that IIIa region was required for high level expression in thepresence of starch or maltose while IIIb region was required for highlevel expression but does not play a role in starch induction. Minetokiet al. further demonstrated that a significant increase in promoteractivity could be observed by introducing multiple copies of region IIIainto the Aspergillus oryzae alpha-glucosidase promoter. In the presentinvention, variants of the Fusarium venenatum glucoamylase promoter wereconstructed which demonstrated that the putative IIIa and IVb regionswere important for expression. In addition, adding IIIa region 35 bpdownstream of the 3792 to 3807 region improved the promoter.

However, the IIIa consensus found in Aspergillus promoters (Minetoki etal., 1996, supra) was not as efficient as the native Fusarium venenatumIIIa promoter sequence.

In a preferred embodiment, the promoter variant has the nucleic acidsequence of SEQ ID NO: 2, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 3, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 4, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 5, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant comprises at leasttwo copies, more preferably at least three copies, and most preferablyat least four copies of the sequence CGGCGTAATTTCGGCC in the Fusariumvenenatum glucoamylase promoter.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 6, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 7, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 8, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 9, or a subsequence thereof. The subsequencepreferably contains at least about 1200 nucleotides, more preferably atleast about 1500 nucleotides, and most preferably at least about 1800nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 10, or a subsequence thereof. Thesubsequence preferably contains at least about 1200 nucleotides, morepreferably at least about 1500 nucleotides, and most preferably at leastabout 1800 nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 11, or a subsequence thereof. Thesubsequence preferably contains at least about 1200 nucleotides, morepreferably at least about 1500 nucleotides, and most preferably at leastabout 1800 nucleotides.

In another preferred embodiment, the promoter variant has the nucleicacid sequence of SEQ ID NO: 12, or a subsequence thereof. Thesubsequence preferably contains at least about 1200 nucleotides, morepreferably at least about 1500 nucleotides, and most preferably at leastabout 1800 nucleotides.

In a preferred embodiment of the methods of the present invention, thepromoter variant, which increases expression of the nucleic acidsequence encoding a biological substance, is selected from the groupconsisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5;and subsequences thereof.

In another preferred embodiment of the methods of the present invention,the promoter variant, which decreases expression of the nucleic acidsequence encoding a biological substance, is selected from the groupconsisting of SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8; SEQ ID NO: 9,SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 12; and subsequencesthereof.

In the methods of the present invention, the promoter variant may alsobe a hybrid promoter comprising a portion of one or more promoters ofthe present invention; a portion of a promoter of the present inventionand a portion of another promoter, e.g., a leader sequence of onepromoter and the transcription start site from the other promoter; or aportion of one or more promoters of the present invention and a portionof one or more other promoters. The other promoter may be any promotersequence which shows transcriptional activity in the fungal host cell ofchoice including a mutant, truncated, and hybrid promoter, and may beobtained from genes encoding extracellular or intracellular polypeptideseither homologous or heterologous to the host cell. The other promotersequence may be native or foreign to the nucleic acid sequence encodingthe biological substance and native or foreign to the cell.

Examples of other promoters useful in the construction of hybridpromoters with the promoter variants of the present invention includethe promoters obtained from the genes for Aspergillus oryzae TAKAamylase, Rhizomucor miehei aspartic proteinase, Aspergillus nigerneutral alpha-amylase, Aspergillus niger acid stable alpha-amylase,Aspergillus niger or Aspergillus awamori glucoamylase (glaA), Rhizomucormiehei lipase, Aspergillus oryzae alkaline protease, Aspergillus oryzaetriose phosphate isomerase, Aspergillus nidulans acetamidase, Fusariumvenenatum amyloglucosidase, Fusarium oxysporum trypsin-like protease (WO96/00787), Trichoderma reesei cellobiohydrolase I, Trichoderma reeseicellobiohydrolase II, Trichoderma reesei endoglucanase I, Trichodermareesei endoglucanase II, Trichoderma reesei endoglucanase III,Trichoderma reesei endoglucanase IV, Trichoderma reesei endoglucanase V,Trichoderma reesei xylanase I, Trichoderma reesei xylanase II,Trichoderma reesei beta-xylosidase, as well as the NA2-tpi promoter (ahybrid of the promoters from the genes for Aspergillus niger neutralalpha-amylase and Aspergillus oryzae triose phosphate isomerase),Fusarium venenatum Daria promote, Fusarium venenatum Quinn promoter,Saccharomyces cerevisiae enolase (ENO-1), Saccharomyces cerevisiaegalactokinase (GAL1), Saccharomyces cerevisiae alcoholdehydrogenase/glyceraldehyde-3-phosphate dehydrogenase (ADH2/GAP), andSaccharomyces cerevisiae 3-phosphoglycerate kinase; and mutant,truncated, and hybrid promoters thereof. Other useful promoters foryeast host cells are described by Romanos et al., 1992, Yeast 8:423-488.

The promoter variant may also be a tandem promoter comprising two morepromoter variants of the present invention or alternatively one or morepromoter variants of the present invention and one or more otherpromoters, such as those exemplified above. The two or more promotersequences of the tandem promoter may simultaneously promote thetranscription of the nucleic acid sequence. Alternatively, one or moreof the promoter sequences of the tandem promoter may promote thetranscription of the nucleic acid sequence at different stages of growthof the cell.

In the methods of the present invention, a hybrid or tandem promoter ofthe present invention will be understood to be foreign to a nucleic acidsequence encoding a biological substance even if the wild-type promoteris native to the nucleic acid sequence. For example, in a tandempromoter consisting of at least two promoters, one of the promoters maybe a the wild-type promoter of the nucleic acid sequence encoding abiological substance.

A promoter variant of the present invention has at least about 20%,preferably at least about 40%, more preferably at least about 60%, morepreferably at least about 80%, more preferably at least about 90%, morepreferably at least about 100%, even more preferably at least about200%, most preferably at least about 300%, and even most preferably atleast about 400% of the promoter activity of the promoter of SEQ ID NO:1.

Biological Substance Encoding Nucleic Acid Sequences

The biological substance encoded by the first nucleic acid sequence maybe native or heterologous to the fungal host cell of interest. Thebiological substance may be any biopolymer or metabolite. The biologicalsubstance may be encoded by a single gene or a series of genes composinga biosynthetic or metabolic pathway or may be the direct result of theproduct of a single gene or products of a series of genes. Thus, theterm “first nucleic acid sequence encoding a biological substance” willbe understood to encompass one or more genes involved in the productionof the biological substance. The term “heterologous biologicalsubstance” is defined herein as a biological substance which is notnative to the host cell; or a native biological substance in whichstructural modifications have been made to alter the native biologicalsubstance.

In the methods of the present invention, the biopolymer may be anybiopolymer. The term “biopolymer” is defined herein as a chain (orpolymer) of identical, similar, or dissimilar subunits (monomers). Thebiopolymer may be, but is not limited to, a nucleic acid, polyamine,polyol, polypeptide (or polyamide), or polysaccharide.

In a preferred embodiment, the biopolymer is a polypeptide. Thepolypeptide may be any polypeptide having a biological activity ofinterest. The term “polypeptide” is not meant herein to refer to aspecific length of the encoded product and, therefore, encompassespeptides, oligopeptides, and proteins. The term “polypeptide” alsoencompasses two or more polypeptides combined to form the encodedproduct. Polypeptides also include hybrid polypeptides, which comprise acombination of partial or complete polypeptide sequences obtained fromat least two different polypeptides wherein one or more may beheterologous to the fungal cell. Polypeptides further include naturallyoccurring allelic and engineered variations of the above-mentionedpolypeptides and hybrid polypeptides.

In a preferred embodiment, the polypeptide is an antibody, antigen,antimicrobial peptide, enzyme, growth factor, hormone, immunodilator,neurotransmitter, receptor, reporter protein, structural protein, andtranscription factor.

In a more preferred embodiment, the polypeptide is an oxidoreductase,transferase, hydrolase, lyase, isomerase, or ligase. In a most preferredembodiment, the polypeptide is an alpha-glucosidase, aminopeptidase,amylase, carbohydrase, carboxypeptidase, catalase, cellulase, chitinase,cutinase, cyclodextrin glycosyltransferase, deoxyribonuclease, esterase,alpha-galactosidase, beta-galactosidase, glucoamylase,glucocerebrosidase, alpha-glucosidase, beta-glucosidase, invertase,laccase, lipase, mannosidase, mutanase, oxidase, pectinolytic enzyme,peroxidase, phospholipase, phytase, polyphenoloxidase, proteolyticenzyme, ribonuclease, transglutaminase, urokinase, or xylanase.

In another preferred embodiment, the polypeptide is a collagen orgelatin.

In another preferred embodiment, the biopolymer is a polysaccharide. Thepolysaccharide may be any polysaccharide, including, but not limited to,a mucopolysaccharide (e.g., heparin and hyaluronic acid) andnitrogen-containing polysaccharide (e.g., chitin). In a more preferredembodiment, the polysaccharide is hyaluronic acid.

In the methods of the present invention, the metabolite may be anymetabolite. The metabolite may be encoded by one or more genes, such asa biosynthetic or metabolic pathway. The term “metabolite” encompassesboth primary and secondary metabolites. Primary metabolites are productsof primary or general metabolism of a cell, which are concerned withenergy metabolism, growth, and structure. Secondary metabolites areproducts of secondary metabolism (see, for example, R. B. Herbert, TheBiosynthesis of Secondary Metabolites, Chapman and Hall, New York,1981).

The primary metabolite may be, but is not limited to, an amino acid,fatty acid, nucleoside, nucleotide, sugar, triglyceride, or vitamin.

The secondary metabolite may be, but is not limited to, an alkaloid,coumarin, flavonoid, polyketide, quinine, steroid, peptide, or terpene.In a preferred embodiment, the secondary metabolite is an antibiotic,antifeedant, attractant, bacteriocide, fungicide, hormone, insecticide,or rodenticide.

The nucleic acid sequence encoding a biological substance of interestmay be obtained from any prokaryotic, eukaryotic, or other source. Forpurposes of the present invention, the term “obtained from” as usedherein in connection with a given source shall mean that the biologicalsubstance is produced by the source or by a cell in which a gene fromthe source has been inserted.

The techniques used to isolate or clone a nucleic acid sequence encodinga biological substance of interest are known in the art and includeisolation from genomic DNA, preparation from cDNA, or a combinationthereof. The cloning of the nucleic acid sequence from such genomic DNAcan be effected, e.g., by using the well known polymerase chain reaction(PCR). See, for example, Innis et al., 1990, PCR Protocols: A Guide toMethods and Application, Academic Press, New York. The cloningprocedures may involve excision and isolation of a desired nucleic acidfragment comprising the nucleic acid sequence encoding the biologicalsubstance, insertion of the fragment into a vector molecule, andincorporation of the recombinant vector into the mutant fungal cellwhere multiple copies or clones of the nucleic acid sequence will bereplicated. The nucleic acid sequence may be of genomic, cDNA, RNA,semisynthetic, synthetic origin, or any combinations thereof.

Nucleic Acid Constructs

The present invention also relates to nucleic acid constructs comprisinga nucleic acid sequence encoding a biological substance operably linkedto at least one promoter variant of the present invention and one ormore control sequences which direct the expression of the codingsequence in a suitable host cell under conditions compatible with thecontrol sequences. Expression will be understood to include any stepinvolved in the production of the biological substance including, butnot limited to, transcription, post-transcriptional modification,translation, post-translational modification, and secretion.

“Nucleic acid construct” is defined herein as a nucleic acid molecule,either single- or double-stranded, which is isolated from a naturallyoccurring gene or which has been modified to contain segments of nucleicacid combined and juxtaposed in a manner that would not otherwise existin nature. The term nucleic acid construct is synonymous with the termexpression cassette when the nucleic acid construct contains a codingsequence and all the control sequences required for expression of thecoding sequence.

An isolated nucleic acid sequence encoding a biological substance may befurther manipulated in a variety of ways to provide for expression ofthe biological substance. Manipulation of the nucleic acid sequenceprior to its insertion into a vector may be desirable or necessarydepending on the expression vector. The techniques for modifying nucleicacid sequences utilizing recombinant DNA methods are well known in theart.

In the methods of the present invention, the nucleic acid sequence maycomprise one or more native control sequences or one or more of thenative control sequences may be replaced with one or more controlsequences foreign to the nucleic acid sequence for improving expressionof the coding sequence in a host cell.

The term “control sequences” is defined herein to include all componentswhich are necessary or advantageous for the expression of a biologicalsubstance of the present invention. Each control sequence may be nativeor foreign to the nucleic acid sequence encoding the biologicalsubstance. Such control sequences include, but are not limited to, aleader, polyadenylation sequence, propeptide sequence, promoter variantof the present invention, signal peptide sequence, and transcriptionterminator. At a minimum, the control sequences include a promotervariant of the present invention, and transcriptional and translationalstop signals. The control sequences may be provided with linkers for thepurpose of introducing specific restriction sites facilitating ligationof the control sequences with the coding region of the nucleic acidsequence encoding a biological substance.

The control sequence may be a suitable transcription terminatorsequence, a sequence recognized by a host cell to terminatetranscription. The terminator sequence is operably linked to the 3′terminus of the nucleic acid sequence encoding the biological substance.Any terminator which is functional in the fungal host cell of choice maybe used in the present invention.

Preferred terminators for filamentous fungal host cells are obtainedfrom the genes for Aspergillus oryzae TAKA amylase, Aspergillus nigerglucoamylase, Aspergillus nidulans anthranilate synthase, Aspergillusniger alpha-glucosidase, and Fusarium oxysporum trypsin-like protease.

Preferred terminators for yeast host cells are obtained from the genesfor Saccharomyces cerevisiae enolase, Saccharomyces cerevisiaecytochrome C (CYC1), and Saccharomyces cerevisiaeglyceraldehyde-3-phosphate dehydrogenase. Other useful terminators foryeast host cells are described by Romanos et al., 1992, supra.

The control sequence may also be a suitable leader sequence, anontranslated region of an mRNA which is important for translation bythe host cell. The leader sequence is operably linked to the 5′ terminusof the nucleic acid sequence encoding the biological substance. Anyleader sequence that is functional in the host cell of choice may beused in the present invention.

Preferred leaders for filamentous fungal host cells are obtained fromthe genes for Aspergillus oryzae TAKA amylase, Aspergillus nidulanstriose phosphate isomerase, Fusarium venenatum trypsin, and Fusariumvenenatum glucoamylase.

Suitable leaders for yeast host cells are obtained from the genes forSaccharomyces cerevisiae enolase (ENO-1), Saccharomyces cerevisiae3-phosphoglycerate kinase, Saccharomyces cerevisiae alpha-factor, andSaccharomyces cerevisiae alcoholdehydrogenase/glyceraldehyde-3-phosphate dehydrogenase (ADH2/GAP).

The control sequence may also be a polyadenylation sequence, a sequenceoperably linked to the 3′ terminus of the nucleic acid sequence andwhich, when transcribed, is recognized by the host cell as a signal toadd polyadenosine residues to transcribed mRNA. Any polyadenylationsequence which is functional in the fungal host cell of choice may beused in the present invention.

Preferred polyadenylation sequences for filamentous fungal host cellsare obtained from the genes for Aspergillus oryzae TAKA amylase,Aspergillus niger glucoamylase, Aspergillus nidulans anthranilatesynthase, Fusarium oxysporum trypsin-like protease, and Aspergillusniger alpha-glucosidase.

Useful polyadenylation sequences for yeast host cells are described byGuo and Sherman, 1995, Molecular Cellular Biology 15: 5983-5990.

The control sequence may also be a signal peptide coding region thatcodes for an amino acid sequence linked to the amino terminus of apolypeptide and directs the encoded polypeptide into the cell'ssecretory pathway. The 5′ end of the coding sequence of the nucleic acidsequence may inherently contain a signal peptide coding region naturallylinked in translation reading frame with the segment of the codingregion which encodes the secreted polypeptide. Alternatively, the 5′ endof the coding sequence may contain a signal peptide coding region whichis foreign to the coding sequence. The foreign signal peptide codingregion may be required where the coding sequence does not naturallycontain a signal peptide coding region. Alternatively, the foreignsignal peptide coding region may simply replace the natural signalpeptide coding region in order to enhance secretion of the polypeptide.However, any signal peptide coding region which directs the expressedpolypeptide into the secretory pathway of a fungal host cell of choicemay be used in the present invention.

Effective signal peptide coding regions for filamentous fungal hostcells are the signal peptide coding regions obtained from the genes forAspergillus oryzae TAKA amylase, Aspergillus niger neutral amylase,Aspergillus niger glucoamylase, Rhizomucor miehei aspartic proteinase,Humicola insolens cellulase, and Humicola lanuginosa lipase.

Useful signal peptides for yeast host cells are obtained from the genesfor Saccharomyces cerevisiae alpha-factor and Saccharomyces cerevisiaeinvertase. Other useful signal peptide coding regions are described byRomanos et al., 1992, supra.

The control sequence may also be a propeptide coding region that codesfor an amino acid sequence positioned at the amino terminus of apolypeptide. The resultant polypeptide is known as a proenzyme orpropolypeptide (or a zymogen in some cases). A propolypeptide isgenerally inactive and can be converted to a mature active polypeptideby catalytic or autocatalytic cleavage of the propeptide from thepropolypeptide. The propeptide coding region may be obtained from thegenes for Saccharomyces cerevisiae alpha-factor, Rhizomucor mieheiaspartic proteinase, and Myceliophthora thermophila laccase (WO95/33836).

Where both signal peptide and propeptide regions are present at theamino terminus of a polypeptide, the propeptide region is positionednext to the amino terminus of a polypeptide and the signal peptideregion is positioned next to the amino terminus of the propeptideregion.

It may also be desirable to add regulatory sequences which allow theregulation of the expression of the biological substance relative to thegrowth of the host cell. Examples of regulatory systems are those whichcause the expression of the gene to be turned on or off in response to achemical or physical stimulus, including the presence of a regulatorycompound.

In yeast, the ADH2 system or GAL1 system may be used. In filamentousfungi, the TAKA alpha-amylase promoter, Aspergillus niger glucoamylasepromoter, Aspergillus oryzae glucoamylase promoter, and Fusariumvenenatum glucoamylase promoter may be used as regulatory sequences.Other examples of regulatory sequences are those which allow for geneamplification. In eukaryotic systems, these include the dihydrofolatereductase gene which is amplified in the presence of methotrexate, andthe metallothionein genes which are amplified with heavy metals. Inthese cases, the nucleic acid sequence encoding the biological substancewould be operably linked with the regulatory sequence.

The present invention also relates to nucleic acid constructs foraltering the expression of a gene encoding a biological substance whichis endogenous to a host cell. The constructs may contain the minimalnumber of components necessary for altering expression of the endogenousgene. In one embodiment, the nucleic acid constructs preferably contain(a) a targeting sequence, (b) a promoter variant of the presentinvention, (c) an exon, and (d) a splice-donor site. Upon introductionof the nucleic acid construct into a cell, the construct inserts byhomologous recombination into the cellular genome at the endogenous genesite. The targeting sequence directs the integration of elements (a)-(d)into the endogenous gene such that elements (b)-(d) are operably linkedto the endogenous gene. In another embodiment, the nucleic acidconstructs contain (a) a targeting sequence, (b) a promoter variant ofthe present invention, (c) an exon, (d) a splice-donor site, (e) anintron, and (f) a splice-acceptor site, wherein the targeting sequencedirects the integration of elements (a)-(f) such that elements (b)-(f)are operably linked to the endogenous gene. However, the constructs maycontain additional components such as a selectable marker.

In both embodiments, the introduction of these components results inproduction of a new transcription unit in which expression of theendogenous gene is altered. In essence, the new transcription unit is afusion product of the sequences introduced by the targeting constructsand the endogenous gene. In one embodiment in which the endogenous geneis altered, the gene is activated. In this embodiment, homologousrecombination is used to replace, disrupt, or disable the regulatoryregion normally associated with the endogenous gene of a parent cellthrough the insertion of a regulatory sequence which causes the gene tobe expressed at higher levels than evident in the corresponding parentcell. The activated gene can be further amplified by the inclusion of anamplifiable selectable marker gene in the construct using methods wellknown in the art (see, for example, U.S. Pat. No. 5,641,670).

In another embodiment in which the endogenous gene is altered,expression of the gene is reduced.

The targeting sequence can be within the endogenous gene, immediatelyadjacent to the gene, within an upstream gene, or upstream of and at adistance from the endogenous gene. One or more targeting sequences canbe used. For example, a circular plasmid or DNA fragment preferablyemploys a single targeting sequence, while a linear plasmid or DNAfragment preferably employs two targeting sequences.

The constructs further contain one or more exons of the endogenous gene.An exon is defined as a DNA sequence which is copied into RNA and ispresent in a mature mRNA molecule such that the exon sequence isin-frame with the coding region of the endogenous gene. The exons can,optionally, contain DNA which encodes one or more amino acids and/orpartially encodes an amino acid. Alternatively, the exon contains DNAwhich corresponds to a 5′ non-encoding region. Where the exogenous exonor exons encode one or more amino acids and/or a portion of an aminoacid, the nucleic acid construct is designed such that, upontranscription and splicing, the reading frame is in-frame with thecoding region of the endogenous gene so that the appropriate readingframe of the portion of the mRNA derived from the second exon isunchanged.

The splice-donor site of the constructs directs the splicing of one exonto another exon. Typically, the first exon lies 5′ of the second exon,and the splice-donor site overlapping and flanking the first exon on its3′ side recognizes a splice-acceptor site flanking the second exon onthe 5′ side of the second exon. A splice-acceptor site, like asplice-donor site, is a sequence which directs the splicing of one exonto another exon. Acting in conjunction with a splice-donor site, thesplicing apparatus uses a splice-acceptor site to effect the removal ofan intron.

The present invention further relates to methods for producing abiological substance comprising (a) cultivating a homologouslyrecombinant cell, having incorporated therein a new transcription unitcomprising a promoter variant of the present invention, an exon, and/ora splice donor site operably linked to a second exon of an endogenousnucleic acid sequence encoding the biological substance, underconditions conducive for production of the biological substance; and (b)recovering the biological substance. The methods are based on the use ofgene activation technology, for example, as described in U.S. Pat. No.5,641,670.

Expression Vectors

The present invention also relates to recombinant expression vectorscomprising a promoter variant of the present invention, a nucleic acidsequence encoding a biological substance, and transcriptional andtranslational stop signals. The various nucleic acid and controlsequences described above may be joined together to produce arecombinant expression vector which may include one or more convenientrestriction sites to allow for insertion or substitution of the promoterand/or nucleic acid sequence encoding the biological substance at suchsites. Alternatively, the nucleic acid sequence may be expressed byinserting the nucleic acid sequence or a nucleic acid constructcomprising the promoter variant and/or sequence into an appropriatevector for expression. In creating the expression vector, the codingsequence is located in the vector so that the coding sequence isoperably linked with a promoter variant of the present invention and oneor more appropriate control sequences for expression.

The recombinant expression vector may be any vector (e.g., a plasmid orvirus) which can be conveniently subjected to recombinant DNA proceduresand can bring about the expression of the nucleic acid sequence. Thechoice of the vector will typically depend on the compatibility of thevector with the host cell into which the vector is to be introduced. Thevectors may be linear or closed circular plasmids.

The vector may be an autonomously replicating vector, i.e., a vectorwhich exists as an extrachromosomal entity, the replication of which isindependent of chromosomal replication, e.g., a plasmid, anextrachromosomal element, a minichromosome, or an artificial chromosome.The vector may contain any means for assuring self-replication.Alternatively, the vector may be one which, when introduced into thehost cell, is integrated into the genome and replicated together withthe chromosome(s) into which it has been integrated. Furthermore, asingle vector or plasmid or two or more vectors or plasmids whichtogether contain the total DNA to be introduced into the genome of thehost cell, or a transposon may be used.

The vectors of the present invention preferably contain one or moreselectable markers which permit easy selection of transformed cells. Aselectable marker is a gene the product of which provides for biocide orviral resistance, resistance to heavy metals, prototrophy to auxotrophs,and the like. Suitable markers for yeast host cells are ADE2, HIS3,LEU2, LYS2, MET3, TRP1, and URA3. Selectable markers for use in afilamentous fungal host cell include, but are not limited to, amdS(acetamidase), argB (ornithine carbamoyltransferase), bar(phosphinothricin acetyltransferase), hygB (hygromycinphosphotransferase), niaD (nitrate reductase), pyrG(orotidine-5′-phosphate decarboxylase), sC (sulfate adenyltransferase),trpC (anthranilate synthase), as well as equivalents thereof. Preferredfor use in an Aspergillus cell are the amdS and pyrG genes ofAspergillus nidulans or Aspergillus oryzae and the bar gene ofStreptomyces hygroscopicus. Preferred for use in a Fusarium cell is thebar, amdS, pyrG, or hygB gene.

The vectors of the present invention preferably contain an element(s)that permits stable integration of the vector into the host cell'sgenome or autonomous replication of the vector in the cell independentof the genome.

For integration into the host cell genome, the vector may rely on thenucleic acid sequence encoding the biological substance or any otherelement of the vector for stable integration of the vector into thegenome by homologous or nonhomologous recombination. Alternatively, thevector may contain additional nucleic acid sequences for directingintegration by homologous recombination into the genome of the hostcell. The additional nucleic acid sequences enable the vector to beintegrated into the host cell genome at a precise location(s) in thechromosome(s). To increase the likelihood of integration at a preciselocation, the integrational elements should preferably contain asufficient number of nucleic acids, such as 100 to 1,500 base pairs,preferably 400 to 1,500 base pairs, and most preferably 800 to 1,500base pairs, which are highly homologous with the corresponding targetsequence to enhance the probability of homologous recombination. Theintegrational elements may be any sequence that is homologous with thetarget sequence in the genome of the host cell. Furthermore, theintegrational elements may be non-encoding or encoding nucleic acidsequences. On the other hand, the vector may be integrated into thegenome of the host cell by non-homologous recombination.

For autonomous replication, the vector may further comprise an origin ofreplication enabling the vector to replicate autonomously in the hostcell in question. Examples of a plasmid replicator useful in a yeastcell are the 2 micron origin of replication, ARS1, ARS4, the combinationof ARS1 and CEN3, and the combination of ARS4 and CEN6. Examples of aplasmid replicator useful in a filamentous fungal cell are AMA1 and ANSI(Gems et al., 1991, Gene 98:61-67; Cullen et al., 1987, Nucleic AcidsResearch 15: 9163-9175; WO 00/24883). Isolation of the AMA1 gene andconstruction of plasmids or vectors comprising the gene can beaccomplished according to the methods disclosed in WO 00/24883. Theorigin of replication may be one having a mutation which makes itsfunctioning temperature-sensitive in the host cell (see, e.g., Ehrlich,1978, Proceedings of the National Academy of Sciences USA 75: 1433).

More than one copy of a nucleic acid sequence encoding a biologicalsubstance may be inserted into the host cell to increase production ofthe gene product. An increase in the copy number of the nucleic acidsequence can be obtained by integrating at least one additional copy ofthe sequence into the host cell genome or by including an amplifiableselectable marker gene with the nucleic acid sequence where cellscontaining amplified copies of the selectable marker gene, and therebyadditional copies of the nucleic acid sequence, can be selected for bycultivating the cells in the presence of the appropriate selectableagent.

The procedures used to ligate the elements described above to constructthe recombinant expression vectors of the present invention are wellknown to one skilled in the art (see, e.g., Sambrook et al., 1989,supra).

Host Cells

The present invention also relates to recombinant host cells, comprisinga promoter variant of the present invention operably linked to a nucleicacid sequence encoding a biological substance, which are advantageouslyused in the recombinant production of the biological substances. Avector comprising a promoter variant of the present invention operablylinked to a nucleic acid sequence encoding a biological substance isintroduced into a host cell so that the vector is maintained as achromosomal integrant or as a self-replicating extra-chromosomal vectoras described earlier. The term “host cell” encompasses any progeny of aparent cell that is not identical to the parent cell due to mutationsthat occur during replication. The choice of a host cell will to a largeextent depend upon the gene encoding the biological substance and itssource.

The host cell may be any fungal cell useful in the methods of thepresent invention. “Fungi” as used herein includes the phyla Ascomycota,Basidiomycota, Chytridiomycota, and Zygomycota (as defined by Hawksworthet al., In, Ainsworth and Bisby's Dictionary of The Fungi, 8th edition,1995, CAB International, University Press, Cambridge, UK) as well as theOomycota (as cited in Hawksworth et al., 1995, supra, page 171) and allmitosporic fungi (Hawksworth et al., 1995, supra).

In a preferred embodiment, the fungal host cell is a yeast cell. “Yeast”as used herein includes ascosporogenous yeast (Endomycetales),basidiosporogenous yeast, and yeast belonging to the Fungi Imperfecti(Blastomycetes). Since the classification of yeast may change in thefuture, for the purposes of this invention, yeast shall be defined asdescribed in Biology and Activities of Yeast (Skinner, F. A., Passmore,S. M., and Davenport, R. R., eds, Soc. App. Bacteriol. Symposium SeriesNO: 9, 1980).

In a more preferred embodiment, the yeast host cell is a Candida,Hansenula, Kluyveromyces, Pichia, Saccharomyces, Schizosaccharomyces, orYarrowia cell.

In a most preferred embodiment, the yeast host cell is a Saccharomycescarlsbergensis, Saccharomyces cerevisiae, Saccharomyces diastaticus,Saccharomyces douglasii, Saccharomyces kluyveri, Saccharomyces norbensisor Saccharomyces oviformis cell. In another most preferred embodiment,the yeast host cell is a Kluyveromyces lactis cell. In another mostpreferred embodiment, the yeast host cell is a Yarrowia lipolytica cell.

In another preferred embodiment, the fungal host cell is a filamentousfungal cell. “Filamentous fungi” include all filamentous forms of thesubdivision Eumycota and Oomycota (as defined by Hawksworth et al.,1995, supra). The filamentous fungi are characterized by a mycelial wallcomposed of chitin, cellulose, glucan, chitosan, mannan, and othercomplex polysaccharides. Vegetative growth is by hyphal elongation andcarbon catabolism is obligately aerobic. In contrast, vegetative growthby yeasts such as Saccharomyces cerevisiae is by budding of aunicellular thallus and carbon catabolism may be fermentative.

In a more preferred embodiment, the filamentous fungal host cell is acell of a species of, but not limited to, Acremonium, Aspergillus,Fusarium, Humicola, Mucor, Myceliophthora, Neurospora, Penicillium,Thielavia, Tolypocladium, or Trichoderma.

In a most preferred embodiment, the filamentous fungal host cell is anAspergillus awamori, Aspergillus foetidus, Aspergillus japonicus,Aspergillus nidulans, Aspergillus niger or Aspergillus oryzae cell. Inanother most preferred embodiment, the filamentous fungal host cell is aFusarium bactridioides, Fusarium cerealis, Fusarium crookwellense,Fusarium culmorum, Fusarium graminearum, Fusarium graminum, Fusariumheterosporum, Fusarium negundi, Fusarium oxysporum, Fusariumreticulatum, Fusarium roseum, Fusarium sambucinum, Fusarium sarcochroum,Fusarium sporotrichioides, Fusarium sulphureum, Fusarium torulosum,Fusarium trichothecioides, or Fusarium venenatum cell. In another mostpreferred embodiment, the filamentous fungal host cell is a Humicolainsolens, Humicola lanuginosa, Mucor miehei, Myceliophthora thermophila,Neurospora crassa, Penicillium purpurogenum, Thielavia terrestris,Trichoderma harzianum, Trichoderma koningii, Trichodermalongibrachiatum, Trichoderma reesei, or Trichoderma viride cell.

In an even most preferred embodiment, the Fusarium venenatum cell isFusarium venenatum A3/5, which was originally deposited as Fusariumgraminearum ATCC 20334 and recently reclassified as Fusarium venenatumby Yoder and Christianson, 1998, Fungal Genetics and Biology 23: 62-80and O'Donnell et al., 1998, Fungal Genetics and Biology 23: 57-67; aswell as taxonomic equivalents of Fusarium venenatum regardless of thespecies name by which they are currently known. In another preferredembodiment, the Fusarium venenatum cell is a morphological mutant ofFusarium venenatum A3/5 or Fusarium venenatum ATCC 20334, as disclosedin WO 97/26330.

Fungal cells may be transformed by a process involving protoplastformation, transformation of the protoplasts, and regeneration of thecell wall in a manner known per se. Suitable procedures fortransformation of Aspergillus host cells are described in EP 238 023 andYelton et al., 1984, Proceedings of the National Academy of Sciences USA81: 1470-1474. Suitable methods for transforming Fusarium species aredescribed by Malardier et al., 1989, Gene 78: 147-156 and WO 96/00787.Yeast may be transformed using the procedures described by Becker andGuarente, In Abelson, J. N. and Simon, M. I., editors, Guide to YeastGenetics and Molecular Biology, Methods in Enzymology, Volume 194, pp182-187, Academic Press, Inc., New York; Ito et al., 1983, Journal ofBacteriology 153: 163; and Hinnen et al., 1978, Proceedings of theNational Academy of Sciences USA 75: 1920.

The present invention is further described by the following exampleswhich should not be construed as limiting the scope of the invention.

EXAMPLES

Chemicals used as buffers and substrates were commercial products of atleast reagent grade.

Strains and Materials

Fungal strains used in the present invention were Fusarium venenatumwild-type strain MLY3 (see U.S. Pat. Nos. 6,066,493 and 6,180,366) andpyrG mutant strain, Fusarium venenatum DLM15. Bacterial strains used togenerate plasmids were Escherichia coli Top 10 (Invitrogen, Carlsbad,Calif.), Epicurian E. coli XL1 Blue competent and supercompetent cells(Stratagene, La Jolla, Calif.), and E coli SEDM1 HKA702 (Stratagene, LaJolla, Calif.).

RA medium was composed per liter of 50 g of succinic acid, 4.9 g ofurea, 1 g of glucose, and 20 ml of 50× Vogels salts.

50× Vogel's Salts was composed per liter of 150 g of sodium citrate, 250g of KH₂PO₄, 10 g of MgSO₄-7H₂O, 20 ml of 25% CaCl₂.2H₂O, 5.0 ml ofbiotin (5 mg per 100 ml of 50% ethanol), and 5 ml of Vogels traceelements (filter sterilized).

Vogel's trace elements solution was composed per liter of 50 g of citricacid, 50 g of ZnSO₄.7H₂O, 10 g of Fe(NH₄)₂(SO₄)₂.6H₂O, 2.5 g ofCuSO₄.5H₂O, 0.5 g of MnSO₄.H₂O, 0.5 g of H₃BO₃, and 0.5 g ofNa₂MoO₄.2H₂O.

Minimal medium transfer and transformation plates (pH 6.5) were composedper liter of 6 g of NaNO₃, 0.52 g of KCL, 1.52 g of KH₂PO₄, 1 ml of Covetrace elements, 20 grams of Noble agar with addition of 20 ml of 50%glucose, 2.5 ml of 20% MgSO₄.7H2O and 20 ml of 0.02% biotin afterautoclaving. Transformation plates contained all of the aboveingredients plus sucrose at a final concentration of 0.8 M.

Cove trace elements solution was composed per liter of 0.04 g ofNa₂B₄O₇.10H₂O, 0.4 g of CuSO₄.5H₂O, 1.2 g of FeSO₄.7H₂O, 0.7 g ofMnSO₄.H₂O, 0.8 g of Na₂MoO₂.2H₂O, and 10 g of ZnSO₄.7H₂O.

Vogels NH₄H2PO₄ plates were composed per liter of 20 ml of 50× Vogelssalts, 15 g of sucrose, 25 g of Noble agar with addition of 50 ml ofNH₄H₂PO₄ (1 M pH 6) after autoclaving.

M400 medium (pH 6) was composed per liter of 50 g of maltodextrin, 2 gof MgSO₄.7H₂O, 2 g KH₂PO₄, 4 g of citric acid, 8 g of yeast extract, 2 gof urea, 0.5 ml of AMG trace elements, and 0.5 g of CaCl₂.

AMG trace elements solution was composed per liter of 14.3 g ofZnSO₄.7H₂O, 2.5 g of CuSO₄.5H₂O, 0.5 g of NiCl₂.6H₂O, 13.8 g ofFeSO₄.7H₂O, 8.5 g of MnSO₄.H₂O, and 3 g of citric acid.

Chlorate plates were composed per liter of 20 ml of Cove salt solution,61.28 g of potassium chlorate, 0.3 g of urea, and 25 g of Noble agar.

Cove salt solution was composed per liter of 26 g of KCl, 26 g ofMgSO₄.7H₂O, 76 g of KH₂PO₄, and 50 ml of Cove trace elements solution.

LB plus ampicillin broth was composed per liter of 10 g of tryptone, 5 gof yeast extract, 5 g of sodium chloride, and 100 mg of ampicillin.

LB plus ampicillin plates were composed of 1 liter of LB plus ampicillinbroth with 15 g of bacto agar.

YP-5% glucose broth was composed per liter of 10 g of yeast extract, 20g of bacto peptone, and 5% glucose.

2XYT plus ampicillin was composed per liter of 16 g of tryptone, 10 g ofyeast extract, 5 g of sodium chloride, and 100 mg of ampicillin.

2XYT plus ampicillin plates were composed per liter of 2XYT+ ampicillinbroth plus 15 g of bacto agar.

NYZ plus broth (pH 7.5) was composed per liter of 5 g of NaCl, 2 g ofMgSO₄.7H₂O, 5 g of yeast extract, 10 g of NZ amine (casein hydrolysate),12.5 ml of 1 M MgCl₂, 12.5 ml of 1 M MgSO₄, and 20 ml of 20% glucose.

NZY top agarose was composed per liter of 5 g of NaCl, 2 g ofMgSO₄.7H₂O, 5 g of yeast extract, 10 g of NZ amine (casein hydrolysate),and 7 g of agarose.

DNA Sequencing

DNA sequencing was done with a Perkin-Elmer Applied Biosystems Model3700 Automatic DNA Sequencer (Perkin-Elmer Applied Biosystems, Inc.,Foster City, Calif.) using dye-terminator chemistry (Giesecke et al.,1992, Journal of Virology Methods 38: 47-60) and the reverse or forwardlac sequencing primer or sequence specific primers.

Example 1 Construction of pDM237

pDM237 (FIG. 2) was constructed to contain a 4.4 kb EcoRI/HindIIIFusarium venenatum niaD fragment cloned into pBluescript SK(−)(Stratagene, La Jolla, Calif.). The niaD insert was composed of a 1.8 kbKpnI/EcoRI fragment from clone F (a genomic niaD clone) and a 2.6 kbKpnI/HindIII fragment from pDM201 (a genomic clone of niaD).

The niaD genomic clones were isolated from the Lambda ZipLox Fusariumvenenatum genomic library described previously (U.S. Pat. No.6,361,973). Clone pDM201 was isolated by probing the library with a 1.1kb Fusarium oxysporum niaD fragment (Diolez et al., 1993, Gene 131:61-67). The Fusarium oxysporum probe was amplified from Fusariumoxysporum genomic DNA using the following primers:

(SEQ ID NO: 13) 5′-ATCGAGGGTGCCAATGTG-3′ (foxy.nia1) (SEQ ID NO: 14)5′-GCCATTTACGACCTCAGC-3′ (foxy.nia2).

The 100 μl PCR reaction contained 10 μg of genomic DNA, 50 pmol of eachprimer, 1× Taq buffer (Boehringer Mannheim, Indianapolis, Ind.), 200 μMeach of dATP, dCTP, dGTP, and dTTP, and 5 units of Pwo DNA polymerase(Boehringer Mannheim, Indianapolis, Ind.). PCR conditions used were 95°C. for 3 minutes followed by 30 cycles at 95° C. for 30 seconds, 50° C.for 1 minute, and 72° C. for 1 minute. The final extension cycle was at72° C. for 5 minutes. The PCR product was subcloned using the TA cloningkit from Invitrogen (Carlsbad, Calif.). The sublcones were checked byrestriction digest with EcoRI and confirmed by nucleotide sequencingusing the M13 universal forward and reverse primers. One of the cloneswas confirmed to contain the 1.1 kb niaD insert and was named pDM197.

To prepare a DIG-labeled probe of the Fusarium oxysporum niaD fragment,pDM197 was digested with EcoRI and a 1.1 kb fragment was isolatedfollowing gel electrophoresis on a 0.8% agarose gel using 40 mMTris-acetate, 1 mM disodium EDTA buffer (TAE) and extraction of the DNAfrom the gel using the QIAquick Gel Extraction Kit (Qiagen, Inc.,Chatsworth, Calif.). The probe was prepared by PCR using the primersfoxy.nia1 and foxy.nia2 described above. The 100 μl PCR reactioncontained 6 ng of 1.1 kb EcoRI niaD fragment, 50 pmol of each primer, 1×Taq buffer (Boehringer Mannheim, Indianapolis, Ind.), 10 μl of 10×DIGlabeling mix (Boehringher Mannheim, Indianapolis, Ind.), and 5 units ofTaq DNA polymerase (Boehringer Mannheim, Indianapolis, Ind.). PCRconditions used were 95° C. for 3 minutes followed by 30 cycles at 95°C. for 30 seconds, 50° C. for 1 minute, and 72° C. for 1 minute. Thefinal extension cycle was at 72° C. for 5 minutes.

Approximately 90,000 plaques from the Fusarium venenatum genomic DNAlibrary were screened by hybridization (Davis et al., 1986, BasicMethods in Molecular Biology, Elsevier Science Publishing Co., Inc., NewYork) with the DIG-labeled probe using medium stringency conditions[i.e., hybridization at 37° C. in DIG Easy hyb (Boehringher Mannheim,Germany); filters washed twice in 2×SSC with 0.1% SDS at roomtemperature for 5 minutes followed by two washes in 0.2×SSC with 0.1%SDS at the same temperature for 15 minutes)]. For detection of theDIG-labeled probe the standard Genius protocol from Boehringher Mannheimwas followed using CPD Star as the substrate following themanufacturer's protocols. Plaques providing hybridization signals werepurified twice on E. coli Y1090ZL cells, and the individual clones weresubsequently excised from the λZipLox vector as pZL1-derivatives(D'Alessio et al., 1992, Focus® 14: 76). DNA sequence analysis revealedthat one of these clones, containing a plasmid designated pDM201,contained the niaD gene, but was missing approximately 400 bp at the 5′end of the open reading frame.

In order to obtain a genomic clone containing the entire niaD openreading frame as well as the promoter, the genomic clone pDM201 was usedto create a probe to a 0.46 kb fragment at the 5′ end of the openreading frame. The probe was prepared by PCR using the followingprimers:

(SEQ ID NO: 15) 5′ CCCCGATAAAGATGGCTGTA 3′ (niaprobe.plus)(SEQ ID NO: 16) 5′ TCGCTAGGCTCTTGGGTGAC 3′ (niaprobe.minus)

The 50 μl PCR reaction contained 6 ng of pDM201, 50 pmol each primer, 1×Taq buffer (Boehringer Mannheim, Indianapolis, Ind.), 5 μl of 10×DIGlabeling mix (Boehringher Mannheim, Indianapolis, Ind.), and 5 units ofTaq DNA polymerase (Boehringer Mannheim, Indianapolis, Ind.). PCRconditions used were 95° C. for 3 minutes followed by 30 cycles at 95°C. for 30 seconds, 50° C. for 1 minute, and 72° C. for 1.5 minutes. Thefinal extension cycle was at 72° C. for 5 minutes.

Approximately 80,000 plaques from the Fusarium venenatum genomic DNAlibrary were screened by hybridization (Davis et al., 1986, supra) withthe DIG-labeled probe using high stringency conditions (i.e.,hybridization at 65° C. in DIG Easy hyb; filters washed twice in 2×SSCwith 0.1% SDS at room temperature for 5 minutes followed by two washesin 0.1×SSC with 0.1% SDS at 65° C. for 15 mintutes). For detection ofthe DIG-labeled probe the standard Genius protocol from BoehringherMannheim was followed using CPD Star as the substrate following themanufacturer's protocols. Plaques yielding hybridization signals werepurified twice on E. coli Y1090ZL cells, and the individual clones weresubsequently excised from the λZipLox vector as pZL1-derivatives. DNAsequence analysis revealed that one of these clones, containing aplasmid designated clone F, contained the niaD gene as well as 1.6 kb ofthe promoter. However, the clone was missing 450 bp at the 3′ end of theopen reading frame.

Plasmid pDM237 (FIG. 2), containing the entire niaD open reading frameas well as the promoter and terminator, was created. pDM237 consisted ofa 4.4 kb EcoRI/HindIII Fusarium venenatum niaD fragment cloned intopBluescript SK(−) (Stratagene, La Jolla, Calif.) constructed asdescribed below. The niaD insert consisted of a 1.8 kb KpnI/EcoRIfragment from clone F and a 2.6 kb KpnI/HindIII fragment from pDM201.Following restriction digests of pDM201 and clone F with KpnI/HindIIIand KpnI/EcoRI; respectively, and electrophoresis on an agarose gelusing TAE buffer, the desired fragments were isolated using a QIA quickgel extraction kit. The plasmid pBluescript SK(−) was digested withEcoRI/HindIII followed by electrophoresis and isolation as describedabove. The 2.9 kb pBluescript SK(−) plasmid was ligated with the 1.8 kbKpnI/EcoRI and the 2.6 kb KpnI/HindIII fragments for three hours at 14°C. followed by transformation of SURE competent cells from Stratagene(La Jolla, Calif.) selecting on 2XYT ampicillin plates. Plasmid DNA wasisolated from clones, and the restriction analysis was used to confirmthat the clone pDM237 contained the desired insert.

Example 2 Construction of pJRoy72

pJRoy72 (FIG. 3) was constructed by ligating a 0.9 kb PCR productcontaining a Thermomyces lanuginosus lipase gene, a 2.1 kb StuI/BspLU11Ifrom pRaMB62-int1 (U.S. Pat. No. 6,361,973) and PmeI/PacI digestedpRamB60 (U.S. Pat. No. 6,361,973). The lipase fragment was amplifiedfrom pDM194 (U.S. Pat. No. 6,361,973) using the following primers:

(SEQ ID NO: 17) 5′-GACTCATGAGGAGCTCCCTTGTGCTGTTC-3′ (SEQ ID NO: 18)5′-TGATTAATTAACCTAAAGACATGTCCCAATTAAC-3′

The 100 μl PCR reaction contained 15 ng of pDM194, 50 pmol of eachprimer, 1×PCR buffer (Perkin-Elmer Corp., Branchburg, N.J.), 250 μM eachof dATP, dCTP, dGTP, and dTTP, and 5 units of Pwo DNA polymerase(Boehringer Mannheim, Indianapolis, Ind.). The PCR conditions used wereone cycle at 94° C. for two minutes, 10 cycles of 94° C. for 30 seconds,55° C. for 45 seconds, and 72° C. for two minutes followed by 17 cyclesat 94° C. for 30 seconds, 55° C. for 45 seconds, and 72° C. for twominutes with an extension of 20 seconds more for each cycle. The finalcycle was 72° C. for 10 minutes. The 0.9 kb PCR product was ethanolprecipitated followed by digestion with PacI and BspHI.

The PmeI/PacI digested pRaMB60, Stul/BspLU111 digested pRaMB62-int1 and0.9 kb PCR product were electrophoresed on a 1% agarose gel using TAEbuffer, and the DNA was purified from the excised band using a Qiaquickkit following the manufacturer's protocol.

To construct pJRoy72, the 5.8 kb PmeI/PacI fragment of pRaMB60 wasligated with the 0.9 kb PacI/BspHI lipase fragment and the 2.1 kbStul/BspLU111 fragment from pRaMB62-int1. The resulting vector, pJRoy72(FIG. 3), contained the Thermomyces lanuginosus lipase gene under thecontrol of the Fusarium venenatum glucoamylase promoter (SEQ ID NO: 1).

Example 3 Construction of pNham1

Plasmid pNham1 (FIG. 4) was constructed using the following strategy: A1.6 kb fragment containing the niaD promoter was isolated by digestingpDM237 with BamHI/EcoRI and a 760 bp fragment containing the niaDterminal region was isolated by digesting pNham3 of Example 5 withBamHI/HindIII. A fragment of approximately 1.6 kb containing theAspergillus oryzae pyrG gene was obtained by digesting pSMO122 (U.S.Pat. No. 5,958,727) with BamHI. A 2.9 kb backbone vector fragment wasgenerated by digesting pBluescript SK(−) with EcoRI and HindIII followedby treatment with shrimp alkaline phosphatase (Boehringer-Mannheim,Germany) to prevent self-ligation. After digestion, all the fragmentswere isolated by electrophoresis on a 0.7% agarose gel using TAE bufferfollowed by excision of the bands containing the desired fragments andisolation of the DNA from the gel using the Qiaquick Gel Extraction Kitfollowing the manufacturer's protocol. All gel-purified fragments wereligated together to construct pNham1 using Rapid DNA Ligation Kit(Boehringer Mannheim, Germany) with the following ligation mix: 2 μl ofBamHI/HindIII fragment from pNham3, 2 μl of BamHI/EcoRI fragment frompDM237, 2 μl of BamHI from pSMO122, 1 μl of pBluescript SK(−), 10 μl of2×T4 DNA dilution buffer, 2 μl of 5×DNA dilution buffer, and 1 μl of T4ligase. The ligation reaction was incubated at room temperature for 30minutes. Epicurian E. coli XL Blue competent cells (Stratagene, LaJolla, Calif.) were transformed, and transformants were selected on 2XYTampicillin plates. Plasmid DNA was isolated from several of thetransformant colonies by inoculating a colony into 2.5 ml of LB mediumsupplemented with ampicillin (100 μg/ml). The tube was incubated at 37°C. for overnight with shaking at 250 rpm. Plasmid DNA was isolated usingthe Qiagen BioRobot following the manufacturer's protocols. The plasmidswere analyzed by restriction enzyme digestion to confirm the correctinserts.

Example 4 Construction of pNham2

Plasmid pNham2 (FIG. 5) was constructed to contain the truncatedFusarium venenatum niaD gene and an expression cassette where theThermomyces lanuginosus lipase gene is sandwiched between the Fusariumvenenatum glucoamylase promoter and the Fusaium oxysporum trypsinterminator. A 1.1 kb fragment containing the terminator of Fusariumoxysporum trypsin gene and a 3.0 kb fragment containing the Thermomuyceslanuginosus lipase/glucoamylase promoter regions were isolated bydigesting pJRoy72 with PacI/ClaI and PacI/NotI, respectively. A 3.6 kbfragment containing a truncated niaD fragment was obtained by digestingpDM237 with XbaI/ClaI. A 3.9 kb fragment containing the backbone vectorwas prepared by digesting pCR2.1®-TOPO® (Invitrogen, Carlsbad, Calif.)with XbaI and NotI followed by treatment with shrimp alkalinephosphatase (Boehringer-Mannheim, Indianapolis, Ind.) to preventself-ligation. After digestion all the fragments were isolated byelectrophoresis on a 0.7% agarose gel using TAE buffer followed byexcision of the bands containing the desired fragments and isolation ofthe DNA from the gel using the Qiaquick Gel Extraction Kit following themanufacturer's protocol.

pNham2 was obtained by ligation of 2 μl of the PacI/ClaI fragment frompJRoy72, 2 μl of the PacI/NotI fragment from pJRoy72, 2 μl of theXbaI/ClaI fragment from pDM237, 1 μl of the XbaI/NotI fragment frompCR2.1®-TOPO®, 1 μl of 10× ligation buffer, and 1 μl of T4 DNA ligaseusing the Rapid DNA Ligation Kit (Boehringer Mannheim, Germany). Theligation reaction was incubated at 14° C. for 24 hours. Epicurian E.coli XL blue competent cells (Stratagene, La Jolla, Calif.) weretransformed, and transformants were selected on LB plates supplementedwith 50 mg of ampicillin per liter. Plasmid DNA was isolated fromseveral of the transformant colonies and analyzed by endonucleasedigestion and by sequencing of pNham2 to confirm the sequence of theglucomylase promoter.

Example 5 Construction of pNham3

A 760 bp fragment of the BamHI/HindIII niaD terminator from pDM237 wasamplified by PCR with the following primers:

5′-GGATCCTTGAATAAGCGTAAATAGGG-3′ (SEQ ID NO: 19)5′-AAGCTTGCTGAGCATTTGACTGCC-3′ (SEQ ID NO: 20)The PCR reaction contained 1 μl of 1:10 dilution of pDM237 (0.3μg/μl-0.35 μg/μl), 5 μl of 10× Taq buffer (Perkin Elmer Corp.,Branchburg, N.J.), 1 μl of 25 mM dNTPs (Boehringer Mannheim,Indianapolis, Ind.), 1 μl of 50 ρmol primer 1, 1 μl of 50 ρmol primer 2,0.5 μl of 5 units/μl Taq polymearse (Perkin Elmer), and 40.5 μl ofdistilled water. The PCR reaction was performed in an Ericomp TwinBlockThermal Cycler with the following cycling parameters and conditions: 1cycle at 95° C. for 3 minutes followed by 25 cycles at 95° C. for 30seconds, 55° C. for 30 seconds, and 72° C. for 1 minute followed by 1cycle at 72° C. for 10 minutes. An aliquot of the PCR reaction waselectrophoresed on a 1% agarose-TAE gel to verify the amplification of a760 bp fragment.

The 760 bp PCR product of the Fusarium venenatum niaD terminator wascloned into pCRII using Topo TA cloning Kit (Invitrogen, Carlsbad,Calif.) following the manufacturer's protocol for cloning andtransformation. Plasmid DNA was isolated from several of thetransformants and sequence analysis was performed to confirm the clonesthat contain the 760 bp insert.

Example 6 Construction of Fusarium venenatum pyrG Mutant DLM15

A 0.78 kb fragment of the Neurospora crassa pyr-4 gene was labeled in aPCR reaction containing digoxigenin (DIG)-labeleddeoxyuridine-triphosphate (dUTP) using the primers described below.

Primer 94-885 (sense): 5′-GTCAGGAAACGCAGCCACAC-3′ (SEQ ID NO: 21)Primer 94-959 (anti-sense): 5′-AGGCAGCCCTTGGACGACAT-3′ (SEQ ID NO: 22)

A 1.1 kb HindIII fragment purified from plasmid pFB6 (Fungal GeneticsStock Center) was used as template. The PCR conditions for the Taqpolymerase reaction were 95° C. for 3 minutes followed by 35 cycles of95° C. for 30 seconds, 55° C. for 1 minute and 72° C. for 1 minute. Afinal extension was performed 5 minutes at 72° C. The DIG-labeled probewas used to screen a genomic library of Fusarium venenatum strain ATCC20334 DNA cloned into lambda vector EMBL4 using the same proceduredescribed in Royer et al., 1995, Bio/Technology 13: 1479-1483. Lambdaphage were plated with E. coli K802 cells (Clonetech, Palo Alto, Calif.)onto LB plates with NZY top agarose. Plaque lifts were made to nylonmembranes (Hybond™ membrane, Amersham Pharmacia Biotech, UK) usingstandard techniques. DNA was bound to the membranes by UV crosslinking.Filters were hybridized with the 0.78 kb DIG-labeled probe describedabove. Hybridization and detection of pyrG clones were performed usingtechniques described in the Boehringer Mannheim Genius™ System User'sGuide. Hybridizations were performed at 42° C. in 5×SSC, 35% formamide,0.1% L-lauroylsarcosine, 0.02% SDS, 1% blocking reagent for nucleic acidhybridization (Boehringer Mannheim, Indianapolis, Ind.). Theconcentration of DIG-labeled probe used was 2.5 ng per ml ofhybridization solution. Hybridizing DNA was immunodetected with analkaline-phosphatase-conjugated anti-digoxigenin antibody and visualizedwith Lumiphos 530, a chemiluminescent substrate (Boehringer Mannheim,Indianapolis, Ind.). DNA preparations were made from putative positivelambda clones using the Qiagen Lambda Midi Kit (QIAGEN, Inc.,Chatsworth, Calif.).

A 3.9 kb genomic EcoRI pyrG fragment was gel purified from one of thelambda clones and cloned into the EcoRI site of pUC118 yielding plasmidpDM156.2 (FIG. 6). The pyrG fragment contained the entire coding regionplus 1.3 kb of the promoter and 1.5 kb of the terminator.

Plasmid pDM222A (FIG. 7) was constructed to create a 2.7 kb deletion atthe pyrG locus. A 3.2 kb PmeI/SwaI Aspergillus nidulans amdS fragmentwith terminal Aspergillus oryzae pyrG repeats (Royer, et al., 1999,Fungal Genetics and Biology 28: 68-78) taken from plasmid pJRoy47.1 wascloned into pDM156.2 to replace a 2.7 kb StuI/EcoRV portion of the pyrGlocus producing pDM222A. This deletion included 0.78 kb of the promoter,the entire pyrG coding region, and 0.8 kb of the terminator region. ThepyrG regions flanking the amdS insert were 0.5 kb at the 5′ end and 0.7kb at the 3′ end. A 4.4 kb EcoRI fragment was gel purified from the pyrGdeletion plasmid pDM222A and used to transform Fusarium venenatum strainMLY3.

To generate spores, 10 to 15 agar plugs from a fresh Fusarium venenatumMLY3 strain (7-14 days) were inoculated into 500 ml of RA medium forapproximately 40 hours at 26° C. with shaking at 150 rpm. Spores wereharvested by filtration through sterile Miracloth (Calbiochem, La Jolla,Calif.) and spun for 20 minutes at 7974×g with Sorvall RC-5B centrifuge.The pellet was rinsed twice with 40 ml of distilled water followed bycentrifugation at 1877×g for 20 minutes with Sorvall RT 6000D. A cellcounting chamber (VWR Scientific, West Chester, Pa.) was used todetermine the number of spores.

Protoplasts for transformation were generated as described below. Amilliliter of fresh spores (2×10⁸/ml) was inoculated into a 500 mlbaffled shake flask containing 100 ml of YP-5% glucose broth andincubated at 23.5° C. for 16 hours at 150 rpm. The culture was filteredthrough sterile Miracloth followed by two rinses with 50 ml of distilledwater and one rinse with sterile 50 ml of 1 M MgSO₄.7H₂O (0.2 μmfiltered). Germlings were collected using a sterile spatula and wereresuspended with 100 mg of NOVOZYME 234™ (Novozymes A/S, Bagsvaerd,Denmark) in 20 ml 1 M MgSO₄7H₂O. After resuspension, the tube wasincubated at 29° C., 90 rpm for 1 hour. Thirty milliliter of 1 Msorbitol was added to the tube followed by centrifugation for 10 minutesat 470×g. The supernatant was discarded, and the pellet was resuspendedin 1 ml of 1 M sorbitol followed by addition of 30 ml of 1 M sorbitol.The tube was centrifuged at 469×g for 5 minutes. The supernatant wasdiscarded, and the pellet was resuspended in 1 ml of 1 M sorbitolfollowed by addition of 30 ml of 1 M sorbitol. Before centrifugation for5 minutes at 470×g, a 100 μl aliquot was transferred to an Eppendorftube containing 900 μl of STC (0.8 M sorbitol, 25 mM, pH 8.0 Tris, 50 mMCaCl₂) to determine the number of protoplasts. The supernatant wasdiscarded and the pellet was resuspended in STC:SPTC (40% PEG, 0.8 Msorbitol, 25 mM Tris pH 8.0, 50 mM CaCl₂):DMSO (9:1:0.1) to a finalconcentration of 5×10⁷ protoplasts/ml. Protoplasts were stored at −80°C. until use.

For transformation the transforming DNA was mixed with 2 ml ofprotoplasts (5×10⁷/ml) in a 50 ml Falcon tube followed by 50 μl ofheparin (5 mg/ml in STC) and 100 μg of DNA. The contents were gentlymixed by rotation, and the tube was incubated on ice for 30 minutes. A200 μl volume of SPTC was slowly added to the tube followed by 10minutes of incubation at room temperature. An additional volume of 20 mlof SPTC was added to the reaction and gently mixed followed by 10minutes of incubation at room temperature. Two ml of the transformationreaction was added to a Falcon tube containing 25 ml of COVE top agaroseplus 10 mM uridine and the contents were mixed by gently inverting thetube. The mixture was then plated onto an underlay containing COVEmedium.

The transformants were transferred to Vogel's acetamide agar plus orminus 10 mM uridine. Transformants which grew poorly on uridine minusmedium were transferred to liquid minimal medium with and without 10 mMuridine. Mycelia were collected from strains which grew well in uridinesupplemented medium but did not grow without uridine. Genomic DNA wasprepared by inoculating three agar plugs from a minimal medium platesupplemented with uridine containing the fungal strain of interest intoa 125 ml flask containing 25 ml of M400 medium. The flask was incubatedat 26° C. for 3 days with shaking at 150 rpm. Fungal mycelia were thenharvested from the culture by filtration through Miracloth followed by 2washes with TE (per liter containing 1 M Tris-HCl pH8, 0.5 M EDTA pH 8).Mycelia were placed in a 15 ml Falcon tube and frozen in liquidnitrogen. Using a mortar and a pestle, frozen mycelia were grounded to afine powder. The fine powder was quickly transferred into a 15 ml Falcontube and a Qiagen DNeasy Plant kit (QIAGEN, Inc., Chatsworth, Calif.)was used to extract the genomic DNA following the manufacturer'sprotocol. Genomic DNA was digested with EcoRI. A Southern blot wasprepared and probed with a 3.2 kb fluoroscein-labeled pyrG fragment. ThepyrG fragment contained the entire coding region plus 1.3 kb of thepromoter and 1.5 kb of the terminator. The Vistra fluorescence kit RPN5751 from Amersham Life Science was used for labeling and themanufacturers instructions were followed for hybridizing and washing theblot. However, CDP-star (Roche Molecular Biochemicals) was used forsignal detection and the blot was exposed to X-ray film instead of usingthe STORM Fluorlmager. Transformants, which yielded the predicted 4.4 kbhybridizing band characteristic of a clean double crossover event, weregrown in liquid minimal medium plus 10 mM uridine for 63 hours at 28°C., 200 rpm. Spores were isolated by micromanipulation on Vogel'sacetamide medium supplemented with 10 mM uridine. One spore isolate wasgrown in RA sporulation medium plus uridine 30 hours at 30° C., 150 rpm.Spores were separated from the mycelia by filtration through sterileMiracloth.

A 100 μl aliquot of the spore stock (9.5×10⁵ spores) was spread ontoeach of 5 fluoroacetamide agar plates plus 10 mM uridine. Colonies whichgrew on fluoroacetamide plates were transferred to both fluoroacetamideand COVE agar. Colonies that grew well on fluoroacetamide and poorly ornot at all on COVE were analyzed further. Spore isolates from three ofthese strains were subjected to Southern blot analysis. Genomic DNA wasisolated as described above, digested with EcoRI, and probed with thepyrG probe described above. Several of the spore isolates yielded a 1.4kb hybridizing band indicating an amdS “loop-out”. One spore isolate waschosen and was designated Fusarium venenatum strain DLM15.

Example 7 Construction of DIG-Labeled Probes for niaD, pyrG, Fusariumoxysporum Trypsin Gene, and Thermomyces lanuginosus Lipase Gene forSouthern Analysis

The DIG-labeled probes for niaD, pyrG, Fusarium oxysporum trypsin gene,and Thermomyces lanuginosus lipase gene were constructed using a PCR DIGProbe Synthesis Kit (Boehringer Mannheim, Indianapolis, Ind.) followingthe manufacturer's guidelines. The primers listed below were used toproduce the DIG-labeled probes for Southern analysis.

Primer 3: 5′-ACAATGTTATCAATCCTCTTA-3′ (SEQ ID NO: 23) Primer 4:5′-TGTCCCATGTTCTCGGTGCTA-3′ (SEQ ID NO: 24) Primer 5:5′-GCCGACGTGACAACCACCAAAGA-3′ (SEQ ID NO: 25) Primer 6:5′-CCACGGGATCAGGAGCAGCATAAA-3′ (SEQ ID NO: 26) Primer 7:5′-GAAGCGTCGAGATGTTCCTTG-3′ (SEQ ID NO: 27) Primer 8:5′-GGCAGACCGATGACTTTGG-3′ (SEQ ID NO: 28) Primer 9:5′-GTTCTTTGTCTCTGCGTGGAC-3′ (SEQ ID NO: 29) Primer 10:5′-GGATATCCGGAATGTTAGGC-3′ (SEQ ID NO: 30)

Primer 3 and 4 were used to generate a 3.5 kb niaD fragment derived fromthe niaD gene of the pDM237. Primer 5 and 6 were used to produce a 719bp pyrG fragment from pNham1. Primer 7 and 8 were used to generate a 756bp Fusarium oxysporum trypsin gene fragment from pNham2. Primer 9 and 10were used to produce an 811 bp Thermomyces lanuginosus lipase fragmentfrom pNham2.

The following components were added to PCR reactions to generateDIG-labeled probes for Southern analysis: 5 μl of PCR 10× buffer, 5 μlof DIG Synthesis Mix (vial 2), 1 μl of upper primer (50 pmol/μl), 1 μlof lower primer (50 pmol/μl), 0.75 μl of Expand™ High Fidelity enzymemix (vial 1), 1 μl of pDM237 or pNham1 or pNham2 (50-100 ng/μl), and35.25 μl of distilled water.

PCR reactions were performed in an Eppendorf MasterCycler with thefollowing cycling parameters and conditions as indicated by therespected DIG probe:

For the niaD probe, 1 cycle at 95° C. for 3 minutes followed by 30cycles at 95° C. for 1 minute, 52.9° C. for 1 minute, and 72° C. for 3½minutes followed by 1 cycle at 72° C. for 10 minutes.

For the pryG probe, 1 cycle at 95° C. for 3 minutes followed by 30cycles at 95° C. for 1 minute, 60.1° C. for 1 minute, and 72° C. for 1minute followed by 1 cycle at 72° C. for 10 minutes.

For the Fusarium oxysporum trypsin gene probe, 1 cycle at 95° C. for 3minutes followed by 30 cycles at 95° C. for 1 minute, 54.9° C. for 1minute, and 72° C. for 1 minute followed by 1 cycle at 72° C. for 10minutes.

For the Thermomyces lanuginosus lipase probe, 1 cycle at 95° C. for 3minutes followed by 30 cycles at 95° C. for 1 minute, 56.8° for 1minute, and 72° C. for 1 minute followed by 1 cycle at 72° C. for 10minutes.

PCR products were resolved on a 0.75% agarose gel in 1×TAE runningbuffer. The amplified DNA fragments were excised from the gel andpurified using a Qiaquick Gel Extraction kit following themanufacturer's protocol.

Example 8 Construction of Fusarium venenatum niaD Mutant

Plasmid pNham1 (Example 3) was used to construct a Fusarium venenatumniaD mutant. pNham1 was linearized with XhoI and EcoRI and transformedinto the Fusarium venenatum pyrG mutant strain DLM15 (Example 6). Forthe transformation, 50 μg of the linearized pNham1 was used pertransformation reaction as described in Example 7. One hundred andfourteen transformants grew on Vogels NH₄H₂PO₄ plates, and fifty of thetransformants were tested for growth on chlorate plates. Forty of thefifty transformants tested for growth on chlorate were resistant tochlorate as expected for a niaD mutant. These 40 chlorate resistancetransformants were further evaluated for their ability to use nitriterather than nitrate as the sole nitrogen source on minimal medium. Allchlorate resistant transformants grew on nitrite as sole nitrogen sourcewhich is a phenotype characteristic of niaD mutants.

Six putative niaD mutant strains were selected to be analyzed andconfirmed by Southern analysis. Genomic DNA was isolated from all sixstrains as follows. Three agar plugs were removed from a minimal mediumplate containing the fungal strain of interest and placed in a 125 mlflask containing 25 ml of M400 medium. The flask was incubated at 26° C.for 3 days with shaking at 150 rpm. Fungal mycelia were then harvestedfrom the culture by filtration through Miracloth followed by 2 washeswith TE (per liter containing 1 M Tris-HCl pH8, 0.5 M EDTA pH 8).Mycelia were placed in a 15 ml Falcon tube and frozen in liquidnitrogen. Using a mortar and a pestle, frozen mycelia were grounded to afine powder. The fine powder was quickly transferred into a 15 ml Falcontube and a Qiagen DNeasy Plant kit (QIAGEN, Inc., Chatsworth, Calif.)was used to extract the genomic DNA following the manufacturer'sprotocol.

For Southern analysis, genomic DNA from the six putative niaD disruptedstrains were digested with PstI, NsiI, and EcoRV and probed with eitherthe 3.6 Kb niaD fragment from pDM237 (Example 8) or with the 780 bp pyrGfragment (Example 8) from pNham1. Genomic DNA from niaD mutants anduntransformed DLM15 strain were digested with Nsi I and Pst I, EcoRV,and BamHI overnight at 37° C. (11 μl of distilled water, 5 μl of genomicDNA (3 μg), 2 μl of 10× buffer, and 2 μl of the restrictionendonucleases). After digestion, each reaction was resolved on a 1%agarose gel using TAE buffer containing 2 μl of ethidium bromide. Thegels were submerged in 250 mM HCl for 10 minutes at room temperaturewith gentle agitation. The gels were rinsed in water for 5 minutes andthen placed into denaturation buffer (0.5 M NaOH, 1.5 M NaCl) and gentlyagitated twice for 15 minutes at room temperature followed by a 5 minuterinse with water. The gels were then submerged in neutralization buffer(1 M Tris pH 8, 1.5 M NaCl) and gently agitated twice for 15 minutes atroom temperature. The DNA was transferred to a Hybond™ membrane usingSchleicher & Schuell Turblotter (Schleicher & Schuell Inc. Keene, N.H.)with 10×SSC (1.5 M NaCl and 1.5 M sodium citrate) overnight.

On day two, the membranes were gently rinsed with 2×SSC for 5 minutesand then crosslinked in an UV Stratalinker™ (Stratagene, La Jolla,Calif.) at 120,000 joules/cm². The dried blots were then pre-hybridizedin a glass tube containing 30 ml of DIG Easy Hyb at 42° C. for at least2 hours. After that time, the prehybridization solution was discardedand replaced with 7.5 ml of fresh DIG Easy Hyb containing 40 μl of gelpurified DIG-labeled probe generated by PCR, which had been denatured ina boiling water bath for 10 minutes. The hybridization tube wasincubated at 42° C. in a Hybaid (National Labnet Company Woodbridge,N.J.) oven overnight.

After hybridization, each blot was washed twice for 5 minutes in 300 mlof 2×SCC, 0.1% SDS solution at room temperature with gentle rotation inthe same hybridization tube and two more washes for 15 minutes in 300 mlof 0.2×SSC, 0.1% SDS solution at 65° C. Each blot was then equilibratedin 150 ml of 1× wash buffer (15 ml 10× wash buffer [Roche Mannheim,Germany] and 135 ml distilled H₂O) with gentle agitation at roomtemperature for 1 minute. The wash buffer was discarded and 100 ml of 1×block solution (10 ml 10× block [Roche Mannheim, Germany], 10 ml 10×maleic acid [Roche Mannheim, Germany], and 80 ml of distilled water) wasadded to each blot followed by gentle agitation at room temperature forat least 60 minutes. The block solution was discarded and each blot wasincubated in 30 ml of anti-digoxigenin-AP solution (diluted 1:20,000 in1× blocking solution) with gentle agitation for 15 minutes. Each blotwas washed twice in 130 ml of 1× wash buffer for 20 minutes with gentleagitation at room temperature. The blots were then equilibrated for 5minutes each in 40 ml of 1× detection buffer (4 ml of 10× detection(Roche) and 36 ml of distilled water) with gentle agitation at roomtemperature. Each blot was placed on an acetate sheet and 1 ml ofchemiluminescent substrate (CDP-Star™ diluted 1:100 in 1× detectionbuffer) was applied onto each blot. The blots were covered with a secondacetate sheet and incubated for 5 minutes at room temperature. The blotswere exposed to X-ray films in a metal cassette for 10-15 minutes oruntil desired exposure was obtained.

Southern analysis demonstrated that three of the six transformants hadthe expected gene replacement at the niaD locus. The three transformantscontained the pyrG gene, which was integrated by a double crossoverevent to disrupt the niaD gene. PstI digested genomic DNA from niaDtransformants produced 869 bp and 1.6 kb bands as well as a third bandof >8.5 kb. The untransformed Fusarium venenatum strain DLM15 produced a3.3 kb band and a >8.5 kb band when probed with the niaD fragment. NsiIdigested genomic DNA produced a 687 bp and a 1.7 kb band as well as athird band of >8.5 kb. The untransformed Fusarium venenatum strain DLM15produced a 680 bp and a >8.5 band when probed with the identical niaDfragment. In addition, the three niaD transformants were digested withEcoRV, which produced a 4.5 kb and a 1.9 kb band when probed either witha niaD fragment or a pyrG fragment. EcoRV digested DNA of theuntransformed Fusarium venenatum strain DLM15 produced three bands of1.2 kb, 1.5 kb, and 4.2 kb when probed with the niaD fragment and nobands were observed when probed with the pyrG fragment.

The following procedure for spore purification was performed twice inorder to obtain a purified fungal strain. Three agar plugs were removedfrom a minimal medium plate containing the fungal strain and placed in a125 ml flask containing 25 ml of RA medium. The flask was incubated at26° C. for 40 hours with shaking at 150 rpm. Fungal spores were thenharvested from the culture by filtration through Miracloth andcentrifuged for 10 minutes at 1877×g with Sorvall RT 6000D centrifuge.The pellet was rinsed twice with 40 ml of distilled water followed bycentrifugation at 1877×g for 20 minutes. Appropriate dilutions of thespores were plated on minimal medium plates to obtain isolated colonies.Individual colonies were transferred to minimal medium plates and grewfor 5-7 day and subsequent spore purification process was repeated.

Fusarium venenatum niaD mutant #3 was selected according to protoplastand lipase yields obtained for all three transformants: niaD mutant #3produced slightly higher observed lipase yield when compared to niaDmutant #2 and niaD mutant #3 rendered a higher number of protoplastswhen compared to niaD mutant #4. Hence, niaD mutant #3 was the selectedstrain used as the host for the analysis of pNham2 and pNham2 variants.

Example 10 Construction of pNham2 Promoter Variants

Thirteen promoter variants of pNham2 were produced by deletion,substitution, and insertion of nucleotide sequences using the StratageneQuikChange™ Site-Directed Mutagenesis Kit (Stratagene Cloning System, LaJolla, Calif.) following the manufacturer's guidelines and using theprimers listed below:

Primer 15: (SEQ ID NO: 31) 5′-CACGAACGCCTGCTCTATAGCGCCAATGAGG-3′Primer 16: (SEQ ID NO: 32) 5′-CCTCATTGGCGCTATAGAGCAGGCGTTCGTG-3′Primer 17: (SEQ ID NO: 33) 5′-CGACCAGACTAAACCATGCGGGGGATTGGGG-3′Primer 18: (SEQ ID NO: 34) 5′-CCCCAATCCCCCGCATGGTTTAGTCTGGTCG-3′Primer 19: (SEQ ID NO: 35)5′-GGCGTAATTTATACCATAGCGGGAAACTCCTGTTTTGTCAAG-3′ Primer 20:(SEQ ID NO: 36) 5-CTTGACAAAACAGGAGTTTCCCGCTATGGTATAAATTACGCC-3′Primer 21: (SEQ ID NO: 37) 5′-CGAACGCCTGCTCTCGTAATTTATACC-3′ Primer 22:(SEQ ID NO: 38) 5′-GGTATAAATTACGAGAGCAGGCGTTCG-3′ Primer 23:(SEQ ID NO: 39) 5′-CTCGGCGTAATTTCGGCCATAGCGCCAATG-3′ Primer 24:(SEQ ID NO: 40) 5′-CATTGGCGCTATGGCCGAAATTACGCCGAG-3′ Primer 25:(SEQ ID NO: 41) 5′-CGCCTGCTCTCGGAAATTTAAATACCATAGCGCC-3′ Primer 26:(SEQ ID NO: 42) 5′-GGCGCTATGGTATTTAAATTTCCGAGAGCAGGCG-3′ Primer 27:(SEQ ID NO: 43) 5′-CGCCTGCTCTCGGAAATTTAACGGCCATAGCGCCAATG-3′ Primer 28:(SEQ ID NO: 44) 5′-CATTGGCGCTATGGCCGTTAAATTTCCGAGAGCAGGCG-3′ Primer 29:(SEQ ID NO: 45) 5′-GCCTGCTCTCGGAAATTTAAAAATTTAACGGCCATAGCGCCAATG-3′Primer 30: (SEQ ID NO: 46)5′-ATTGGCGCTATGGCCGTTAAATTTTTAAATTTCCGAGAGCAGGCG-3′ Primer 31:(SEQ ID NO: 47) 5′-CGAACGCCTGCTCTTATATGCCGGGCGCAAATAGCGCCAATGAG-3′Primer 32: (SEQ ID NO: 48)5′-CTCATTGGCGCTATTTGCGCCCGGCATATAAGAGCAGGCGTTCG-3′ Primer 33:(SEQ ID NO: 49) 5′-CGAACGCCTGCTCTATTCGTAATTTATACC-3′ Primer 34:(SEQ ID NO: 50) 5′-GGTATAAATTACGAATAGAGCAGGCGTTCG-3′ Primer 35:(SEQ ID NO: 51) 5′-CGTAATTTATACCATAGCGAAGGGTCTTTAGGAAACTCCTGTTTTGT C-3′Primer 36: (SEQ ID NO: 52)5′-GACAAAACAGGAGTTTCCTAAAGACCCTTCGCTATGGTATAAATTAC G-3′ Primer 37:(SEQ ID NO: 53) 5′-CTCCTGTTTTGTCGGCGTAATTTCGGCCGTTGGGTCATG-3′ Primer 38:(SEQ ID NO: 54) 5′-CATGACCCAACGGCCGAAATTACGCCGACAAAACAGGAG-3′

Primers 15 and 16 were used to create pNham2-Del.1, which contained adeletion spanning the nucleotide sequence of CGGCGTAATTTATACC atpositions −158 to −143 upstream of the Fusarium venenatum glucoamylasepromoter which corresponded to nucleotides 1952 to 1967 of SEQ ID NO: 1(SEQ ID NO: 68).

Primers 17 and 18 were used to create pNham2-Del.2, which contained adeletion spanning the nucleotide sequence of CGGGAGAGTGTCAAAT atpositions −272 to −257 upstream of the Fusarium venenatum glucoamylasepromoter which corresponded to nucleotides 1838 to 1853 of SEQ ID NO: 1(SEQ ID NO: 2).

Primers 19 and 20 were used to create pNham2-Del.3, which contained adeletion spanning the nucleotide sequence of CCAATGAGGGC at positions−134 to −124 upstream of the Fusarium venenatum glucoamylase promoterwhich corresponded to nucleotides 1974 to 1984 of SEQ ID NO: 1 (SEQ IDNO: 6).

Primers 21 and 22 were used to create pNham2-Del.4, which contained adeletion spanning the CGG nucleotides of the sequence ofCGGCGTAATTTATACC at positions −158 to −156 upstream of the Fusariumvenenatum glucoamylase promoter which corresponded to nucleotides 1952to 1954 of SEQ ID NO: 1 (SEQ ID NO: 7).

Primers 23 and 24 were used to create pNham2-Sub.1, which contained asubstitution of ATA with a CGG triplet located at positions −147 to −145upstream of the Fusarium venenatum glucoamylase promoter whichcorresponded to nucleotides 1963 to 1965 of SEQ ID NO: 1. Thissubstitution produced a promoter variant comprising the sequence ofCGGCGTAATTTCGGCC (SEQ ID NO: 3).

Primers 25 and 26 were used to create pNham2-Sub.2, which contained theconsensus of AAATTTAA within the sequence of CGGCGTAATTTATACC. Thissubstitution produced a promoter variant containing the sequence ofCGGAAATTTAAATACC at positions −155 to −148 of the Fusarium venenatumglucoamylase promoter which corresponded to nucleotides 1955 to 1962 ofSEQ ID NO: 1 (SEQ ID NO: 8).

Primers 27 and 28 were used to create pNham2-Sub.3, which contained thesequence CGGAAATTTAACGGCC substituted at positions −155 through −145from the start codon. This substitution corresponds to nucleotides 1955to 1965 of SEQ ID NO: 1 (SEQ ID NO: 9).

Primers 29 and 30 were used to create pNham2-Ins.1, which contained aninsertion of the consensus of AAATTTAA within pNham2-Sub.3 variantlocated between −148 to −147 which corresponded to nucleotides 1962 to1963 of SEQ ID NO: 1 (SEQ ID NO:10). This insertion produced a variantcomprising the sequence of CGGAAATTTAAAAATTTAACGG.

Primers 31 and 32 were used to create pNham2-Sub.4, which contained thesubstituted sequence of TATATGCCGGGCGCAA located at positions −158 to−143 of the Fusarium venenatum glucoamylase promoter which correspondedto nucleotides 1952 to 1967 of SEQ ID NO: 1 (SEQ ID NO: 69).

Primers 33 and 34 were used to create pNham2-Sub.5, which contained thesequence ATT substituted for CGG at positions −158 to −156 of theFusarium venenatum glucoamylase promoter which corresponded tonucleotides 1952 to 1954 of SEQ ID NO: 1 (SEQ ID NO: 11). Thissubstitution produced a variant comprising the sequence ofATTCGTAATTTATACC.

Primers 35 and 36 were used to create pNham2-Sub.6, which contained thesubstituted sequence of AAGGGTCTTTA located at positions −134 to −124 ofthe Fusarium venenatum glucoamylase promoter which corresponded tonucleotides 1974 to 1984 of SEQ ID NO: 1 (SEQ ID NO: 12).

pNham2-Sub.7 was created using pNham2-Del.2 with primer 23 and 24 tosubstitute ATA with a CGG triplet located at positions −147 to −145upstream of the Fusarium venenatum glucoamylase promoter whichcorresponded to nucleotides 1963 to 1965 of SEQ ID NO: 1 (SEQ ID NO: 4).

Primers 37 and 38 were used to create pNham2-Sub.8 (from pNham2-Sub.1)which contained an additional copy of the sequence CGGCGTAATTTCGGCC (SEQID NO: 70) substituted at positions −108 through −93 of the Fusariumvenenatum glucoamylase promoter which corresponded to nucleotides 2002to 2017 of SEQ ID NO: 1 (SEQ ID NO: 5).

All pNham2 Fusarium venenatum glucoamylase promoter variants generatedby site-directed mutagenesis were confirmed by sequencing. Sequenceanalyses were performed on the Fusarium venenatum glucoamylase promoter,the Thermomyces lanuginosus lipase gene, and part of the Fusariumoxysporum trypsin terminator in the pNham2 variants. The followingprimers were used to confirm the sequence of the variants:

Primer 39. 5′-CGAACAGACGCCTCCGAAGAG-3′ (SEQ ID NO: 55) Primer 40.5′-GTGACATCGCCCACTCCAGAG-3′ (SEQ ID NO: 56) Primer 41.5′-GATGTTACGACGTGGGCCTGA-3′ (SEQ ID NO: 57) Primer 42.5′-ACGCCGCAGCCGAGAC-3′ (SEQ ID NO: 58) Primer 43. 5′-CTGGTTATTGCCGCCG-3′(SEQ ID NO: 59) Primer 44. 5′-TACCGCATTACCCACACCAAT-3′ (SEQ ID NO: 60)Primer 45. 5′-TGTTCGGCAGACAGATAACTG-3′ (SEQ ID NO: 61) Primer 46.5′-GCCCAAGACGACAGAGACGAC-3′ (SEQ ID NO: 62) Primer 47.5′-ATGACCTCAACATCTACCCGG-3′ (SEQ ID NO: 63)

Example 11 Analysis of Fusarium venenatum Glucoamylase Promoter Variants

The Fusarium venenatum niaD mutant was transformed with the wild-typepNham2 and its variants described in Example 10 to evaluate thedifferences in lipase yields obtained when a single copy of theconstruct is integrated at the niaD locus. The procedure fortransformation described in Example 7 was followed and 100 pg of DNA foreach variant was used per reaction followed by selection on minimalplates with a nitrite source. Transformants were selected on minimalmedium plates containing nitrite as the sole source of nitrogen. Onlythose transformants which contain a functional niaD gene were able togrow due to integration of the expression plasmid.

Southern analysis was performed on several transformants of pNham2 orglucoamylase promoter variants thereof to determine the copy numberintegrated at the niaD locus as described in Example 8. Genomic DNA ofseveral transformants for each variant was isolated as described inExample 8 and was digested with NheI and MunI. Functional niaDtransformants containing a single copy of the pNham2 integrated at theniaD locus produced 4.5 kb and 9.5 kb bands when probed with the trypsingene fragment described in Example 7. Transformants with multiple copiesof the plasmid produced 4.5 kb and 9.5 kb bands as well as a third bandof 11.5 kb which corresponds to the size of pNham2. The untransformedniaD mutant strain does not contain any bands when probed with theFusarium oxysporum trypsin gene fragment. In addition, the Southernblots were probed with a lipase fragment (Example 7). Single integrantsof pNham2 should contain only a 9.5 kb band when probed with the lipasefragment probe. Multiple integrants should contain the 9.5 kb band aswell as a second band of 11.5 kb. The untransformed niaD strain did notproduce any bands when probed with the lipase fragment.

Functional niaD transformants containing a single copy of the pNham2 orvariants were spore purified (as described in Example 9) twice beforelipase yields were assessed. A minimum of five transformants for eachvariant with a single copy of plasmid integrated was selected forcomparison of lipase activity. Each transformant was grown in 3 separateshake flasks and assayed in triplicate for lipase activity. A 25 mlvolume of M400 medium in a 125 ml flask was inoculated with 2 or 4 plugsderived from a 5-7 day plate. All flasks were incubated for 7 days at28° C. with shaking at 200 rpm. On day 4 and 7, a 1.5 ml sample of eachculture was taken and spun at 13,720×g for 30 minutes with Sorvall MC12V table centrifuge. Supernatants were transferred into a centrifugetube and stored at −20° C. until the lipase assay was performed.

The lipase activity was performed using the following method. Thesubstrate used in the analysis was p-nitrophenyl butyrate (4 ml of 990μl of DMSO, 0.1 M MOPS, and 10 μl of p-nitrophenyl butyrate). A volumeof 100 μl of substrate was added to 100 μl of enzyme (diluted in 0.1 MMOPS pH 7.5, 4 μM CaCl₂) in a 96 well microtiter plates. Lipase activitywas determined by using a standard curve generated using LIPOLASE™(Thermomyces lanuginosus lipase, Novozymes, A/S, Bagsvaerd, Denmark) at0.1, 0.2 0.4, 0.6, 0.8. 0.9, and 1 LU/ml. Using a microplate reader,lipase activity was measured at 405 nm for 5 minutes at 25° C.

The relative lipase activity obtained for wild-type pNham2 and itspromoter variants are shown in Table 1. For each variant the relativemean of lipase activity is shown as well as the p value from a t-test todetermine the probability that the lipase yields for a given variantwere the same as those for the wild type pNham2. The lower the p valuethe higher the probability that the populations are different.

TABLE 1 Lipase activity by Fusarium venenatum functional niaDtransformants # Transformants Relative Mean lipase Strain Screenedactivity (LU/ml) Prob > [t] pNham2 5 1.0 — pNham2-Del.1 7 0.87 0.127 pNham2-Del.2 9 1.41 0.0005 pNham2-Del.3 7 0.34 0.0002 pNham2-Del.4 70.64 0.0059 pNham2-Sub.1 6 3.01 1.2E−05 pNham2-Sub.2 7 0.62 0.0022pNham2-Sub.3 6 0.75 0.0140 pNham2-Ins.1 7 0.51 0.0004 pNham2-Sub.4 71.01 0.9210 pNham2-Sub.5 6 0.40 0.0002 pNham2-Sub.6 5 0.25 7.5E−05pNham2-Sub.7 8 2.72 9.9E−06 pNham2-Sub.8 5 6.04 1.8E−10

Plasmid pNham2-Del.1 contained the deleted putative region IIIa showedno significant change in lipase activity as compared to the wild typeplasmid pNham2. pNham2-Del.2 showed a slight increase in lipaseactivity. Both pNham2-Del.3 and pNham2-Del.4 showed significant decreasein lipase activity as compared to the wild-type.

pNham2-Sub.1 showed a significant increase in lipase activity byapproximately 3-fold when a CGG triplet is substituted at positions −147to −145 of the Fusarium venenatum glucoamylase promoter.

pNham2-Sub.(2-3) and pNham2-Ins.4 showed significant reduction in lipaseactivity.

Substitution analyses of pNham2 Sub.4-6 variants were performed todetermine whether the lipase yields obtained with pNham2-Del.1, 3, and 4were due to position effects or the deletion of important promoterelements. There was no significant difference in lipase activity whencomparing pNham2-Sub.4 to pNham2-Del.1 and wild-type pNham2. Hence,pNham2-Sub.4 substantiates that the result of pNham2-Del.1 variant wasnot caused by position effect.

The findings of pNham2-Sub.5 and 6 substantiate the results ofpNham2-Del. 3 and 4. Thus, it suggested that the deleted nucleotides arepromoter elements, which may be responsible for high-level expression ofthe glucoamylase promoter.

pNham2-Sub.7 variant was created to test for an additive effect inexpression level. pNham2-Sub.7 variant was constructed by combining themutations in pNham2-Del.2 and pNham2-Sub.1. There was no additive effectshown by pNham2-Sub.7 in terms of lipase activity. In fact, there was nosignificant change in expression observed between pNham2-Sub.7 andpNham2-Sub.1.

With pNham2-Sub.8, which contained an additional CGGCGTAATTTCGGCC (SEQID NO: 70) at positions −108 to −93 of the glucoamylase promoter, a sixfold increase in lipase yield was observed in comparison to pNHam2. Thisfinding suggests that the improvement of the glucoamylase promoteractivity can be achieved by the introduction of multiple copies ofCGGCGTAATTTCGGCC (SEQ ID NO: 70) upstream of the start codon.

Example 12 Construction of a DIG-Labeled Histone/Lipase Hybrid Probe forNorthern Analysis

A histone/lipase hybrid probe was produced using the following set ofprimers:

Primer 11: (SEQ ID NO: 64) 5′-TCTGGAGTGGGCGATGTCA-3′ Primer 12:(SEQ ID NO: 65) 5′-ACCAGTGGACTTGCGGGCGTACCCATTTCCACGCAGGTC-3′ Primer 13:(SEQ ID NO: 66) 5′-GACCTGCGTGGAAATGGGTACGCCCGCAAGTCCACTGGT-3′ Primer 14:(SEQ ID NO: 67) 5′-GGATGGCGCAGAGGTTGGTG-3′

Primers 11 and 12 were used to generate a 320 bp histone fragmentderived from a cDNA H3 histone fragment (WO 2000/56762). Primers 13 and14 were used to produce a 320 bp lipase fragment from pNham2. Primers 11and 14 were used to generate a 620 bp histone/lipase fragment from thePCR products of the histone and lipase reactions.

PCR components used for generating the histone and lipase fragment wereas follows: Histone or lipase fragment: 1 μl of DNA (histone cDNA orpNham2) approx. 50 ng, 5 μl of 10× Taq buffer (Roche), 1 μl of 25 mMdNTPs (Boehringer Mannheim, Indianapolis, Ind.), 1 μl of 50 pmol primer11 or 12, 1 μl of 50 pmol primer 13 or 14, 1 μl of 5 units/μl Taqpolymerase (Roche), and 40 μl of distilled water. The cycling parametersand conditions for PCR were as follows: Histone or Lipase fragments: 1cycle at 95° C. for 3 minutes followed by 25 cycles at 95° C. for 30seconds, 60° C. for 30 seconds, and 72° C. for 1 minute followed by 1cycle at 72° C. for 10 minutes.

The PCR Dig Probe Synthesis Kit was used to generate the histone/lipasehybrid probe with the following components: 5 μl of PCR 10× buffer, 5 μlof Dig Synthesis Mix, 1 μl of primer 11 (50 ρmol/μl), 1 μl of primer 14(50 ρmol/μl), 1 μl of Expand™ High Fidelity enzyme mix, 1 μl of thehistone PCR product, 1 μl of the lipase PCR product, and 35 μl ofdistilled water.

The PCR reaction was performed in an Eppendorf MasterCycler with thefollowing cycling parameters and conditions: 1 cycle at 95° C. for 3minutes followed by 30 cycles at 95° C. for 1 minute, 60° C. for 1minute, and 72° C. for 1 minute followed by 1 cycle at 72° C. for 10minutes. The 640 bp PCR product was resolved on a 0.75% agarose gelusing TAE running buffer, excised from the gel, and purified using aQiaquick Gel Extraction kit following the manufacturer's protocol.

Example 13 Northern Analysis of Transformants Containing a Single Copyof the pNham2 Variant Constructs

Northern analysis was performed on a number of pNham2 promoter variantsto determine if the differences in lipase yields observed between thetransformants were due to differences in the amount of lipase mRNAtranscripts present in the cell. Two transformants were chosen for eachof six pNham2 variants.

Three agar plugs were removed from a minimal medium plate containing thefungal strain of interest and placed in a 125 ml flask containing 25 mlof M400 medium. The flask was incubated at 28° C. for 3 days withshaking at 200 rpm. Fungal mycelia were then removed from the cultureand used for RNA extraction. The Bio 101 FastRNA Kit RED (Qbiogene,Inc., Carlsbad, Calif.) was used to extract RNA from the myceliafollowing the manufacturer's protocol.

Ten micrograms of total RNA from each transformant were aliquoted into amicrocentrifuge tube and the content was dried by speed vacuum withmedium heat until the volume was approximately 5 μl. A 15 μl volume ofNorthernMAX™ Gel Loading Solution (AMBION, Austin, Tex.) was added toeach sample and vortexed to resuspend. Samples were heated in boilingwater for 2 minutes, then quickly spun in a microfuge and chilled onice.

Samples were loaded onto a 1.5% formaldehyde agarose gel in MOPS buffer(Amersco Solon, Ohio), and the gel was run at 100 volts until thebromophenol blue dye migrated approximately three-fourths down the gellength. The formaldehyde gel was prepared by mixing 1.5 g agarose, 10 ml10×MOPS buffer and 85 ml H₂O in a beaker. The agarose was dissolved byheating and then cooling to 50° C. with an addition of 5 μl of EtBr and5.4 ml 37% formaldehyde. The gel was rinsed with DEPC-treated water toremove formaldehyde, then transferred to a HyBond N+ membrane overnightat 4° C. using a Schleicher & Schuell Turboblotter (Schleicher &Schuell, Keene, N.H.) and 10×SSC buffer.

Following transfer, the membrane was dried in a vacuum oven at 80° C.for 10 minutes. The membrane was scanned using a STORM 860 Phosphoimager(Molecular Dynamics Piscataway, N.J.) with blue fluorescent mode at 1000PMT voltage to image the RNA on the membrane for subsequentquantitation. Then, the membrane was rinsed twice with 2×SSC buffer for5 minutes with gentle agitation and crosslinked in a UV Stratalinker(Stratagene, La Jolla, Calif.).

The prehybridization and hybridization procedures for Northern analysiswere performed as previously described for Southern analysis (Example8). However, the blot was equilibrated in Buffer A (0.3 M NaCl, 0.1 MTris-HCl, at pH 7.5) prior to detection. Following detection, themembrane was exposed to ECF substrate (Amersham Pharmacia Biotech.,Buckinghamshire, England) overnight. The quantification of both histoneand lipase mRNA levels was determined by using the STORM 860Phosphoimager and Image Quant (version 5.0) program. The resultsobtained are shown in Table 2.

TABLE 2 Northern analysis of pNham2 variants Mean Ratio of lipase toMean relative lipase Strain histone mRNA level activity (LU/ml) pNham20.22 1.0 pNham2-Del.1 0.23 0.87 pNham2-Del.2 0.33 1.41 pNham2-Del.3 0.140.34 pNham2-Del.4 0.19 0.64 pNham2-Sub.1 0.63 3.01 pNham2-Sub.2 0.180.62 pNham2-Sub.5 0.12 0.40 pNham2-sub.8 1.19 6.04Table 2 shows there was no difference in the lipase to histone mRNAratio between wild-type and pNham2-Del. 1 which was consistent with therelatively equivalent lipase yields observed. In contrast, there weresignificant differences between other pNham2 variants when compared tothe wild-type pNham2. The increased lipase mRNA transcript level inpNham2-Del.2 and pNham2-Sub.1 correlated well with the increased lipaseyields observed when compared to pNham2. This correlation suggested thattranscriptional efficiency of the glucoamylase promoter accounted forthe increase in lipase yields. The reduction of lipase mRNA levelsobserved in pNham2-Del.3-Del.4 and pNham2-Sub.2 correlated well with thedecreased lipase yields. These findings indicated that transcriptionalcontrol accounts for the reduced lipase yield due to the deletion of theCGG and CCAATGAGGGC, and the addition of AAATTTAA consensus sequence didnot lead to an increase in expression.

Deposit of Biological Material

The following biological material has been deposited under the terms ofthe Budapest Treaty with the Agricultural Research Service PatentCulture Collection, Northern Regional Research Center, 1815 UniversityStreet, Peoria, Ill., 61604, and given the following accession numbers:

Deposit Accession Number Date of Deposit E. coli TOP10 (pECO3) NRRLB-30067 Oct. 27, 1998

The strain has been deposited under conditions that assure that accessto the culture will be available during the pendency of this patentapplication to one determined by the Commissioner of Patents andTrademarks to be entitled thereto under 37 C.F.R. §1.14 and 35 U.S.C.§122. The deposit represents substantially pure culture of the depositedstrain. The deposit is as required by foreign patent laws in countrieswherein counterparts of the subject application, or its progeny arefiled. However, it should be understood that the availability of adeposit does not constitute a license to practice the subject inventionin derogation of patent rights granted by governmental action.

The invention described and claimed herein is not to be limited in scopeby the specific embodiments herein disclosed, since these embodimentsare intended as illustrations of several aspects of the invention. Anyequivalent embodiments are intended to be within the scope of thisinvention. Indeed, various modifications of the invention in addition tothose shown and described herein will become apparent to those skilledin the art from the foregoing description. Such modifications are alsointended to fall within the scope of the appended claims. In the case ofconflict, the present disclosure including definitions will control.

Various references are cited herein, the disclosures of which areincorporated by reference in their entireties.

What is claimed is:
 1. A method for producing a polypeptide, comprising:(a) cultivating a fungal host cell in a medium conducive for theproduction of the polypeptide, wherein the fungal host cell comprises afirst nucleic acid sequence encoding the polypeptide operably linked toa second nucleic acid sequence comprising a tandem promoter comprisingat least SEQ ID NO: 2; and (b) isolating the polypeptide from thecultivation medium.
 2. The method of claim 1, wherein the fungal hostcell contains one or more copies of the first nucleic acid sequence. 3.The method of claim 1, wherein the fungal host cell contains one copy ofthe first nucleic acid sequence.
 4. The method of claim 1, wherein thepolypeptide is selected from the group consisting of an antigen, enzyme,growth factor, hormone, immunodilator, neurotransmitter, receptor,reporter protein, structural protein, and transcription factor.
 5. Themethod of claim 1, wherein the polypeptide is native or foreign to thefungal host cell.
 6. The method of claim 1, wherein the tandem promotercomprises SEQ ID NO: 2 and one or more promoters selected from the groupconsisting of SEQ ID NO: 3, SEQ ID NO: 4, and SEQ ID NO:
 5. 7. Themethod of claim 1, wherein the tandem promoter comprises at least twocopies of SEQ ID NO:
 2. 8. An isolated tandem promoter comprising atleast SEQ ID NO:
 2. 9. The tandem promoter of claim 8, wherein thetandem promoter comprises SEQ ID NO: 2 and one or more promotersselected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, andSEQ ID NO:
 5. 10. The tandem promoter of claim 8, wherein the tandempromoter comprises at least two copies of SEQ ID NO:
 2. 11. A nucleicacid construct comprising a nucleic acid sequence encoding a polypeptideoperably linked to the promoter variant of claim
 8. 12. A recombinantexpression vector comprising the nucleic acid construct of claim
 11. 13.A recombinant host cell comprising the nucleic acid construct of claim11.
 14. A method for producing a polypeptide, comprising (a) cultivatinga homologously recombinant cell, having incorporated therein anintroduced transcription unit comprising the tandem promoter of claim 8,an exon, and/or a splice donor site operably linked to a second exon ofan endogenous nucleic acid sequence encoding the polypeptide, underconditions conducive for production of the polypeptide; and (b)recovering the polypeptide.